Variant report

Variant	esv3327360
Chromosome Location	chr8:104152001-104154549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:104154460-104154461	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:104153174-104153548	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr8:104153079-104153587	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr8:104153600-104153750	HRE	kidney:	n/a	chr8:104153712-104153722
5	CTCF	chr8:104152982-104153106	MCF-7	breast:	n/a	chr8:104153031-104153044 chr8:104153031-104153044
6	CTCF	chr8:104153672-104153678	Fibrobl	skin:	n/a	n/a
7	CTCF	chr8:104153660-104153810	WERI-Rb-1	eye:	n/a	chr8:104153712-104153722
8	CTCF	chr8:104153640-104153790	WERI-Rb-1	eye:	n/a	chr8:104153712-104153722
9	CTCF	chr8:104152980-104153130	SK-N-SH_RA	brain:	n/a	chr8:104153031-104153044 chr8:104153031-104153044
10	CTCF	chr8:104153040-104153190	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr8:104153660-104153810	BE2_C	brain:	n/a	chr8:104153712-104153722
12	CTCF	chr8:104153000-104153150	GM12865	blood:	n/a	chr8:104153031-104153044 chr8:104153031-104153044
13	CTCF	chr8:104153020-104153170	SAEC	small airway:	n/a	chr8:104153031-104153044 chr8:104153031-104153044
14	CTCF	chr8:104153640-104153790	AG04449	skin:	n/a	chr8:104153712-104153722
15	CTCF	chr8:104153637-104153750	SK-N-SH_RA	brain:	n/a	chr8:104153712-104153722
16	CTCF	chr8:104153040-104153190	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr8:104153630-104153762	H1-hESC	embryonic stem cell:	n/a	chr8:104153712-104153722
18	CTCF	chr8:104153820-104153970	BE2_C	brain:	n/a	n/a
19	CTCF	chr8:104153015-104153060	MCF-7	breast:	n/a	chr8:104153031-104153044 chr8:104153031-104153044
20	CTCF	chr8:104153679-104153724	Fibrobl	skin:	n/a	chr8:104153712-104153722
21	CTCF	chr8:104153564-104153892	H1-hESC	embryonic stem cell:	n/a	chr8:104153712-104153722
22	GABPA	chr8:104152897-104153213	H1-hESC	embryonic stem cell:	n/a	chr8:104153041-104153050
23	GABPA	chr8:104152829-104153287	H1-hESC	embryonic stem cell:	n/a	chr8:104153041-104153050
24	JUN	chr8:104153732-104154051	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAX	chr8:104153335-104153826	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr8:104153058-104154089	U87	brain:	n/a	n/a
27	POLR2A	chr8:104152875-104153303	U87	brain:	n/a	n/a
28	POLR2A	chr8:104152757-104153262	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr8:104153540-104154064	U87	brain:	n/a	n/a
30	POLR2A	chr8:104152894-104153274	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr8:104152857-104153798	IMR90	lung:	n/a	n/a
32	POLR2A	chr8:104151974-104153028	U87	brain:	n/a	n/a
33	POLR2A	chr8:104152875-104153254	U87	brain:	n/a	n/a
34	POLR2A	chr8:104153686-104153711	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr8:104152297-104152718	U87	brain:	n/a	n/a
36	POLR2A	chr8:104153084-104154083	U87	brain:	n/a	n/a
37	RAD21	chr8:104153463-104153859	H1-hESC	embryonic stem cell:	n/a	chr8:104153713-104153727
38	RAD21	chr8:104153528-104153920	SK-N-SH_RA	brain:	n/a	chr8:104153713-104153727
39	RAD21	chr8:104152853-104153983	H1-hESC	embryonic stem cell:	n/a	chr8:104153713-104153727
40	RAD21	chr8:104153462-104153919	H1-hESC	embryonic stem cell:	n/a	chr8:104153713-104153727
41	RAD21	chr8:104153626-104153803	SK-N-SH_RA	brain:	n/a	chr8:104153713-104153727
42	RAD21	chr8:104152991-104153263	IMR90	lung:	n/a	n/a
43	RAD21	chr8:104152927-104153228	SK-N-SH_RA	brain:	n/a	n/a
44	SIN3A	chr8:104152982-104153709	H1-hESC	embryonic stem cell:	n/a	chr8:104152990-104153001 chr8:104153097-104153108
45	SPI1	chr8:104153614-104154004	HL-60	blood:	n/a	chr8:104153790-104153803
46	SPI1	chr8:104153702-104153838	K562	blood:	n/a	chr8:104153790-104153803
47	TBP	chr8:104152574-104153617	H1-hESC	embryonic stem cell:	n/a	n/a
48	UBTF	chr8:104152952-104153188	K562	blood:	n/a	n/a
49	USF2	chr8:104152311-104152338	HepG2	liver:	n/a	n/a
50	YY1	chr8:104152885-104153263	H1-hESC	embryonic stem cell:	n/a	chr8:104152961-104152975 chr8:104153024-104153038 chr8:104153026-104153035 chr8:104153002-104153013 chr8:104153023-104153034 chr8:104153050-104153064 chr8:104153023-104153032 chr8:104152961-104152970

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104152244-104152294	HRCEpiC	kidney:	n/a
2	chr8:104153592-104153642	SK-N-MC	brain:	n/a
3	chr8:104152244-104152294	HRCEpiC	kidney:	n/a
4	chr8:104153592-104153642	SK-N-MC	brain:	n/a
5	chr8:104153637-104153687	HEK293	kidney:	embryo
6	chr8:104152588-104152638	GM12892	blood:	n/a
7	chr8:104152588-104152638	SK-N-MC	brain:	n/a
8	chr8:104153627-104153677	CMK	blood:	n/a
9	chr8:104152244-104152294	AG10803	skin:	n/a
10	chr8:104153148-104153198	PrEC	prostate:	n/a
11	chr8:104153829-104153879	GM12892	blood:	n/a
12	chr8:104153173-104153223	U87	brain:	n/a
13	chr8:104152754-104152804	MCF-7	breast:	n/a
14	chr8:104152750-104152800	HUVEC	blood vessel:	n/a
15	chr8:104153753-104153803	HMEC	breast:	n/a
16	chr8:104153148-104153198	ovcar-3	ovarian:	n/a
17	chr8:104152244-104152294	HCPEpiC	choroid plexus:	n/a
18	chr8:104152279-104152329	Caco-2	colon:	n/a
19	chr8:104153173-104153223	HEK293	kidney:	embryo
20	chr8:104153637-104153687	HRPEpiC	eye:	n/a
21	chr8:104153643-104153693	Caco-2	colon:	n/a
22	chr8:104153148-104153198	SKMC	muscle:	n/a
23	chr8:104152588-104152638	HMEC	breast:	n/a
24	chr8:104152754-104152804	PANC-1	pancreas:	n/a
25	chr8:104152279-104152329	HUVEC	blood vessel:	n/a
26	chr8:104152279-104152329	NB4	blood:	n/a
27	chr8:104152279-104152329	AoSMC	blood vessel:	n/a
28	chr8:104152588-104152638	HepG2	liver:	n/a
29	chr8:104153627-104153677	HCPEpiC	choroid plexus:	n/a
30	chr8:104153643-104153693	SK-N-SH	brain:	n/a
31	chr8:104153592-104153642	GM19239	blood:	n/a
32	chr8:104153627-104153677	K562	blood:	n/a
33	chr8:104154149-104154199	Jurkat	blood:	n/a
34	chr8:104153148-104153198	HCT-116	colon:	n/a
35	chr8:104153829-104153879	BJ	skin:	n/a
36	chr8:104153592-104153642	MCF-7	breast:	n/a
37	chr8:104153627-104153677	GM06990	blood:	n/a
38	chr8:104152244-104152294	GM19239	blood:	n/a
39	chr8:104152279-104152329	AG09309	skin:	n/a
40	chr8:104153592-104153642	NH-A	brain:	n/a
41	chr8:104152279-104152329	AG09319	gingival:	n/a
42	chr8:104152244-104152294	PrEC	prostate:	n/a
43	chr8:104152244-104152294	GM06990	blood:	n/a
44	chr8:104153827-104153877	AG04450	lung:	fetal
45	chr8:104152754-104152804	HRCEpiC	kidney:	n/a
46	chr8:104153767-104153817	AoSMC	blood vessel:	n/a
47	chr8:104154149-104154199	NH-A	brain:	n/a
48	chr8:104153637-104153687	Jurkat	blood:	n/a
49	chr8:104152750-104152800	GM12878	blood:	n/a
50	chr8:104152754-104152804	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104152186..104155681-chr8:104309748..104312108,3	MCF-7	breast:
2	chr8:104153176..104156099-chr8:104164228..104166566,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf56-4	chr8:104153482-104153570	NR_027071

Variant related genes	Relation type
BAALC	TF binding region
C8orf56	TF binding region
BAALC	CpG island
C8orf56	CpG island
ENSG00000164930	chromatin interactions
ENSG00000247081	chromatin interactions
ENSG00000164929	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562116081	chr8:104152071-104152072	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs79620164	chr8:104152087-104152088	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547624860	chr8:104152090-104152091	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs7014008	chr8:104152091-104152092	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs533254971	chr8:104152097-104152098	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188076571	chr8:104152133-104152134	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs570045482	chr8:104152136-104152137	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542005253	chr8:104152167-104152168	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs372888264	chr8:104152179-104152180	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs138827807	chr8:104152194-104152195	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs556398982	chr8:104152196-104152197	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs568299987	chr8:104152202-104152203	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535631285	chr8:104152216-104152217	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554058340	chr8:104152245-104152246	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs180977197	chr8:104152279-104152280	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs7014597	chr8:104152280-104152281	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145977929	chr8:104152290-104152291	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs138919262	chr8:104152325-104152326	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs543080146	chr8:104152339-104152340	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs562395352	chr8:104152382-104152383	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs142941884	chr8:104152393-104152394	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs77495104	chr8:104152397-104152398	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs549926472	chr8:104152482-104152483	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs4734688	chr8:104152484-104152485	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs559527118	chr8:104152509-104152510	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs533217502	chr8:104152542-104152543	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs551479711	chr8:104152551-104152552	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs570077426	chr8:104152553-104152554	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs80153282	chr8:104152580-104152581	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs549151379	chr8:104152586-104152587	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564240742	chr8:104152637-104152638	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs3041481	chr8:104152674-104152675	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs397836232	chr8:104152702-104152703	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs532746908	chr8:104152715-104152716	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs568343395	chr8:104152754-104152755	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs535755175	chr8:104152817-104152818	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377119155	chr8:104152833-104152834	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs546211376	chr8:104152849-104152850	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186133638	chr8:104152867-104152868	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs373372359	chr8:104152869-104152870	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs539512890	chr8:104153003-104153004	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs557813293	chr8:104153027-104153028	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs62527606	chr8:104153028-104153029	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543402318	chr8:104153047-104153048	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535758352	chr8:104153055-104153056	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs192372910	chr8:104153073-104153074	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs3736043	chr8:104153137-104153138	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375144018	chr8:104153149-104153150	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368139550	chr8:104153164-104153165	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs553438961	chr8:104153180-104153181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104146800-104152600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:104148400-104152200	Enhancers	Brain Hippocampus Middle	brain
3	chr8:104149000-104153200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr8:104149600-104152200	Enhancers	Brain Angular Gyrus	brain
5	chr8:104150000-104152600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:104150200-104152200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:104150200-104152400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:104150200-104152600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:104150400-104152200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr8:104150600-104152800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr8:104150600-104152800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:104150800-104152200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr8:104150800-104152200	Weak transcription	Pancreas	Pancrea
14	chr8:104150800-104152200	Weak transcription	Right Ventricle	heart
15	chr8:104150800-104153000	Enhancers	Primary B cells from peripheral blood	blood
16	chr8:104151000-104152200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr8:104151000-104152600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:104151000-104152600	Weak transcription	Ovary	ovary
19	chr8:104151200-104152200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:104151400-104153000	Enhancers	Primary B cells from cord blood	blood
21	chr8:104151600-104152200	Enhancers	Brain Anterior Caudate	brain
22	chr8:104151600-104152200	Enhancers	Brain Cingulate Gyrus	brain
23	chr8:104151600-104152400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr8:104151600-104152600	Weak transcription	Right Atrium	heart
25	chr8:104151800-104152200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:104151800-104152200	Weak transcription	Brain Substantia Nigra	brain
27	chr8:104151800-104152600	Active TSS	Primary hematopoietic stem cells	blood
28	chr8:104152000-104152200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:104152000-104152400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:104152000-104152600	Enhancers	Spleen	Spleen
31	chr8:104152000-104153000	Enhancers	Fetal Brain Male	brain
32	chr8:104152200-104152400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
33	chr8:104152200-104152400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:104152200-104152400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:104152200-104152400	Bivalent/Poised TSS	Adipose Nuclei	Adipose
36	chr8:104152200-104152400	Flanking Active TSS	Right Ventricle	heart
37	chr8:104152200-104152600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:104152200-104152600	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr8:104152200-104152600	Flanking Active TSS	Brain Hippocampus Middle	brain
40	chr8:104152200-104152600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr8:104152200-104152600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:104152200-104152800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:104152200-104152800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr8:104152200-104152800	Flanking Active TSS	Brain Angular Gyrus	brain
45	chr8:104152200-104152800	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr8:104152200-104152800	Enhancers	Pancreas	Pancrea
47	chr8:104152200-104153000	Bivalent Enhancer	Esophagus	oesophagus
48	chr8:104152200-104153000	Enhancers	Gastric	stomach
49	chr8:104152200-104153800	Active TSS	Fetal Brain Female	brain
50	chr8:104152200-104154000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell

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