Variant report

Variant	esv2553332
Chromosome Location	chr1:63151211-63152937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:63151020-63151226	K562	blood:	n/a	n/a
2	BHLHE40	chr1:63151475-63151537	K562	blood:	n/a	n/a
3	CEBPB	chr1:63151355-63151635	K562	blood:	n/a	n/a
4	CEBPB	chr1:63151342-63151608	HepG2	liver:	n/a	n/a
5	CEBPD	chr1:63150964-63151535	K562	blood:	n/a	n/a
6	CUX1	chr1:63151340-63151401	K562	blood:	n/a	n/a
7	EGR1	chr1:63151104-63151399	K562	blood:	n/a	n/a
8	EP300	chr1:63151047-63151452	K562	blood:	n/a	n/a
9	EP300	chr1:63150891-63151374	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr1:63151053-63151336	SK-N-SH_RA	brain:	n/a	n/a
11	FOS	chr1:63151070-63151323	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr1:63150992-63151350	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA1	chr1:63150942-63151665	PBDE	blood:	n/a	n/a
14	GATA2	chr1:63151063-63151675	SH-SY5Y	brain:	n/a	n/a
15	GATA3	chr1:63150861-63151880	SK-N-SH	brain:	n/a	n/a
16	GATA3	chr1:63150889-63151414	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr1:63150758-63151859	SK-N-SH	brain:	n/a	n/a
18	JUN	chr1:63151737-63152356	HepG2	liver:	n/a	chr1:63152175-63152188 chr1:63152176-63152185
19	JUND	chr1:63151122-63151435	K562	blood:	n/a	n/a
20	JUND	chr1:63151730-63152358	HepG2	liver:	n/a	chr1:63152176-63152185
21	MAZ	chr1:63151220-63151324	K562	blood:	n/a	n/a
22	MAZ	chr1:63152926-63154654	IMR90	lung:	n/a	n/a
23	MXI1	chr1:63152116-63154856	SK-N-SH	brain:	n/a	n/a
24	MXI1	chr1:63152706-63154756	IMR90	lung:	n/a	n/a
25	MXI1	chr1:63152933-63153487	Hela-S3	cervix:	n/a	n/a
26	MYC	chr1:63151145-63151564	K562	blood:	n/a	n/a
27	MYC	chr1:63151310-63151453	K562	blood:	n/a	n/a
28	PBX3	chr1:63150918-63151458	SK-N-SH	brain:	n/a	n/a
29	PBX3	chr1:63150860-63151510	SK-N-SH	brain:	n/a	n/a
30	POLR2A	chr1:63151122-63151469	K562	blood:	n/a	n/a
31	POLR2A	chr1:63152466-63152556	ProgFib	skin:	n/a	n/a
32	POLR2A	chr1:63152914-63154755	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr1:63152635-63152657	ProgFib	skin:	n/a	n/a
34	POLR2A	chr1:63152870-63154627	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr1:63151570-63151732	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr1:63152925-63154594	H1-neurons	neurons:	n/a	n/a
37	POLR2A	chr1:63151002-63151315	SK-N-SH	brain:	n/a	n/a
38	POLR2A	chr1:63151286-63151583	HepG2	liver:	n/a	n/a
39	POLR2A	chr1:63152580-63152602	ProgFib	skin:	n/a	n/a
40	RCOR1	chr1:63152200-63154891	IMR90	lung:	n/a	n/a
41	RCOR1	chr1:63151337-63151444	K562	blood:	n/a	n/a
42	RCOR1	chr1:63151086-63151587	K562	blood:	n/a	n/a
43	REST	chr1:63152764-63154855	H1-neurons	neurons:	n/a	chr1:63153977-63153987 chr1:63154116-63154136 chr1:63154134-63154147
44	STAT1	chr1:63152426-63152441	GM12878	blood:	n/a	n/a
45	TAL1	chr1:63151099-63151444	K562	blood:	n/a	n/a
46	TCF12	chr1:63150858-63151642	SK-N-SH	brain:	n/a	n/a
47	TCF12	chr1:63150862-63151497	SK-N-SH	brain:	n/a	n/a
48	TEAD4	chr1:63150969-63151515	K562	blood:	n/a	n/a
49	TEAD4	chr1:63151132-63151460	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63151692-63151742	GM19239	blood:	n/a
2	chr1:63151692-63151742	RPTEC	kidney:	n/a
3	chr1:63151692-63151742	HL-60	blood:	n/a
4	chr1:63151692-63151742	HepG2	liver:	n/a
5	chr1:63151692-63151742	HNPCEpiC	eye:	n/a
6	chr1:63151692-63151742	K562	blood:	n/a
7	chr1:63151692-63151742	SKMC	muscle:	n/a
8	chr1:63151692-63151742	MCF-7	breast:	n/a
9	chr1:63151692-63151742	HRE	kidney:	n/a
10	chr1:63151692-63151742	SAEC	small airway:	n/a
11	chr1:63151692-63151742	GM12891	blood:	n/a
12	chr1:63151692-63151742	PrEC	prostate:	n/a
13	chr1:63151692-63151742	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:63151692-63151742	HIPEpiC	eye:	n/a
15	chr1:63151692-63151742	AG09319	gingival:	n/a
16	chr1:63151692-63151742	Hepatocyte	liver:	n/a
17	chr1:63151692-63151742	GM12878	blood:	n/a
18	chr1:63151692-63151742	NB4	blood:	n/a
19	chr1:63151692-63151742	HRCEpiC	kidney:	n/a
20	chr1:63151692-63151742	HEEpiC	esophagus:	n/a
21	chr1:63151692-63151742	U87	brain:	n/a
22	chr1:63151692-63151742	Jurkat	blood:	n/a
23	chr1:63151692-63151742	NHDF-neo	bronchial:	n/a
24	chr1:63151692-63151742	HUVEC	blood vessel:	n/a
25	chr1:63151692-63151742	NHBE	bronchial:	n/a
26	chr1:63151692-63151742	GM06990	blood:	n/a
27	chr1:63151692-63151742	HAEpiC	amniotic membrane:	n/a
28	chr1:63151692-63151742	BJ	skin:	n/a
29	chr1:63151692-63151742	AG10803	skin:	n/a
30	chr1:63151692-63151742	Hela-S3	cervix:	n/a
31	chr1:63151692-63151742	ovcar-3	ovarian:	n/a
32	chr1:63151692-63151742	ECC-1	luminal epithelium:	n/a
33	chr1:63151692-63151742	HCM	heart:	n/a
34	chr1:63151692-63151742	HEK293	kidney:	embryo
35	chr1:63151692-63151742	ProgFib	skin:	n/a
36	chr1:63151692-63151742	SK-N-SH	brain:	n/a
37	chr1:63151692-63151742	BE2_C	brain:	n/a
38	chr1:63151692-63151742	NH-A	brain:	n/a
39	chr1:63151692-63151742	PANC-1	pancreas:	n/a
40	chr1:63151692-63151742	Caco-2	colon:	n/a
41	chr1:63151692-63151742	IMR90	lung:	fetal
42	chr1:63151692-63151742	HCPEpiC	choroid plexus:	n/a
43	chr1:63151692-63151742	H1-hESC	embryonic stem cell:	embryo
44	chr1:63151692-63151742	GM12892	blood:	n/a
45	chr1:63151692-63151742	T-47D	breast:	n/a
46	chr1:63151692-63151742	CMK	blood:	n/a
47	chr1:63151692-63151742	HMEC	breast:	n/a
48	chr1:63151692-63151742	HCF	heart:	n/a
49	chr1:63151692-63151742	PFSK-1	brain:	n/a
50	chr1:63151692-63151742	AG09309	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:63146913..63149001-chr1:63152180..63153818,3	MCF-7	breast:
2	chr1:63151590..63154458-chr1:63248689..63250715,2	K562	blood:
3	chr1:63151590..63154458-chr1:63248689..63251365,3	K562	blood:
4	chr1:63141617..63143983-chr1:63151351..63153918,2	MCF-7	breast:
5	chr1:63144223..63146231-chr1:63150074..63152820,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000235545	TF binding region
ENSG00000235545	CpG island
ENSG00000125703	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560362796	chr1:63151216-63151217	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs527733091	chr1:63151248-63151249	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs74076907	chr1:63151257-63151258	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188992672	chr1:63151324-63151325	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150229972	chr1:63151389-63151390	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs138720407	chr1:63151396-63151397	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs550865959	chr1:63151495-63151496	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs555857999	chr1:63151526-63151527	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74520993	chr1:63151530-63151531	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs569088226	chr1:63151544-63151545	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148936635	chr1:63151550-63151551	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145545661	chr1:63151595-63151596	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572845906	chr1:63151602-63151603	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138097302	chr1:63151622-63151623	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555074382	chr1:63151626-63151627	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142687575	chr1:63151669-63151670	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376232720	chr1:63151670-63151671	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1168115	chr1:63151678-63151679	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145986035	chr1:63151705-63151706	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138684380	chr1:63151713-63151714	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531247552	chr1:63151714-63151715	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114265104	chr1:63151736-63151737	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs141200970	chr1:63151747-63151748	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201040350	chr1:63151790-63151791	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116475209	chr1:63151802-63151803	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs1185240	chr1:63151829-63151830	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373594458	chr1:63151836-63151837	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377019132	chr1:63151837-63151838	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371485710	chr1:63151839-63151840	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200884213	chr1:63152156-63152157	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs77897785	chr1:63152158-63152159	Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150751978	chr1:63152201-63152202	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543061176	chr1:63152208-63152209	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs77346467	chr1:63152213-63152214	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76754302	chr1:63152225-63152226	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61778364	chr1:63152228-63152229	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375403095	chr1:63152242-63152243	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561289295	chr1:63152252-63152253	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs139017225	chr1:63152284-63152285	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550927539	chr1:63152286-63152287	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374263881	chr1:63152288-63152289	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569149865	chr1:63152289-63152290	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533199676	chr1:63152312-63152313	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551275844	chr1:63152340-63152341	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566618995	chr1:63152347-63152348	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs181091306	chr1:63152377-63152378	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs149868760	chr1:63152381-63152382	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566960184	chr1:63152397-63152398	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs147145613	chr1:63152504-63152505	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556487349	chr1:63152510-63152511	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63112400-63152400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:63113600-63152800	Weak transcription	Primary B cells from cord blood	blood
3	chr1:63138000-63153000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:63141400-63152600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:63142800-63152400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:63143000-63151400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:63143000-63152400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:63143000-63153000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:63147600-63152600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:63148200-63152600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:63148400-63152600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr1:63148600-63151400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr1:63148600-63151400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:63148600-63153000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr1:63148800-63152200	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:63148800-63152800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:63148800-63152800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr1:63149000-63151400	Weak transcription	Brain Hippocampus Middle	brain
19	chr1:63149000-63152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:63149000-63152800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:63149600-63152600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:63150000-63153000	Enhancers	Liver	Liver
23	chr1:63150200-63151400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:63150200-63151400	Enhancers	NHLF	lung
25	chr1:63150200-63151800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:63150200-63151800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr1:63150200-63152200	Enhancers	Muscle Satellite Cultured Cells	--
28	chr1:63150200-63152400	Enhancers	A549	lung
29	chr1:63150200-63152800	Enhancers	Adipose Nuclei	Adipose
30	chr1:63150200-63152800	Enhancers	Fetal Brain Male	brain
31	chr1:63150200-63153000	Enhancers	Fetal Lung	lung
32	chr1:63150400-63152400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:63150600-63151400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:63150600-63151400	Enhancers	Fetal Kidney	kidney
35	chr1:63150600-63151600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:63150600-63151600	Flanking Active TSS	Brain Germinal Matrix	brain
37	chr1:63150600-63151800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:63150600-63152400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:63150600-63152400	Enhancers	NH-A	brain
40	chr1:63150600-63152800	Enhancers	Stomach Mucosa	stomach
41	chr1:63150800-63151400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:63150800-63151600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:63150800-63151600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr1:63150800-63151600	Flanking Active TSS	Fetal Brain Female	brain
45	chr1:63150800-63151600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr1:63150800-63151600	Enhancers	Small Intestine	intestine
47	chr1:63150800-63151600	Enhancers	Spleen	Spleen
48	chr1:63150800-63151600	Flanking Active TSS	HepG2	liver
49	chr1:63150800-63151800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:63150800-63151800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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