Variant report

Variant	nsv823860
Chromosome Location	chr6:150183482-150186226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:753)
CpG islands
(count:916)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150186002-150186469	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:150186071-150186474	K562	blood:	n/a	n/a
3	ATF3	chr6:150184956-150185229	K562	blood:	n/a	n/a
4	BACH1	chr6:150185045-150185235	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:150186131-150186460	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:150186225-150186514	K562	blood:	n/a	n/a
7	BACH1	chr6:150184213-150184496	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:150185584-150185784	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr6:150186116-150186415	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:150184918-150185520	K562	blood:	n/a	chr6:150185246-150185262 chr6:150185420-150185436
11	BHLHE40	chr6:150184309-150185887	HepG2	liver:	n/a	chr6:150185246-150185262 chr6:150184350-150184366 chr6:150185420-150185436
12	BHLHE40	chr6:150186110-150186409	K562	blood:	n/a	n/a
13	BHLHE40	chr6:150186087-150186340	GM12878	blood:	n/a	n/a
14	BRCA1	chr6:150185423-150185667	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr6:150185381-150185579	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:150184224-150184578	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr6:150185712-150185900	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr6:150185006-150185026	HepG2	liver:	n/a	n/a
19	CBX3	chr6:150185290-150185821	K562	blood:	n/a	n/a
20	CCNT2	chr6:150184406-150185741	K562	blood:	n/a	n/a
21	CEBPB	chr6:150184008-150185779	Hela-S3	cervix:	n/a	chr6:150184098-150184115
22	CEBPB	chr6:150185534-150185774	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:150184506-150184864	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:150183995-150184329	IMR90	lung:	n/a	chr6:150184098-150184115
25	CEBPD	chr6:150185180-150185852	HepG2	liver:	n/a	n/a
26	CHD1	chr6:150185016-150185767	H1-hESC	embryonic stem cell:	n/a	chr6:150185305-150185315
27	CHD1	chr6:150184564-150184631	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr6:150181747-150185902	IMR90	lung:	n/a	chr6:150185305-150185315
29	CHD2	chr6:150185291-150185744	K562	blood:	n/a	chr6:150185305-150185315
30	CHD2	chr6:150184306-150185780	Hela-S3	cervix:	n/a	chr6:150185305-150185315
31	CHD2	chr6:150184360-150185768	HepG2	liver:	n/a	chr6:150185305-150185315
32	CHD2	chr6:150184816-150184881	K562	blood:	n/a	n/a
33	CHD2	chr6:150184939-150184984	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:150185444-150185849	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr6:150185640-150185907	A549	lung:	n/a	n/a
36	CREB1	chr6:150184371-150184800	A549	lung:	n/a	n/a
37	CREB1	chr6:150186041-150186427	GM12878	blood:	n/a	n/a
38	CREB1	chr6:150184813-150186117	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:150184842-150185688	K562	blood:	n/a	n/a
40	CREB1	chr6:150184887-150186443	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr6:150184102-150186511	HepG2	liver:	n/a	n/a
42	CREB1	chr6:150184810-150185950	A549	lung:	n/a	n/a
43	CTCF	chr6:150186150-150186365	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr6:150185097-150185116	K562	blood:	n/a	n/a
45	CTCF	chr6:150186160-150186310	HepG2	liver:	n/a	n/a
46	CTCF	chr6:150184552-150184591	ProgFib	skin:	n/a	n/a
47	CTCF	chr6:150185020-150185170	GM12865	blood:	n/a	n/a
48	CTCF	chr6:150186180-150186330	AG04449	skin:	n/a	n/a
49	CTCF	chr6:150186200-150186350	AG04450	lung:	n/a	n/a
50	CTCF	chr6:150185600-150185750	GM12872	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150185854-150185904	SK-N-SH_RA	brain:	n/a
2	chr6:150185854-150185904	SK-N-SH_RA	brain:	n/a
3	chr6:150184916-150184966	MCF-7	breast:	n/a
4	chr6:150184916-150184966	T-47D	breast:	n/a
5	chr6:150185499-150185549	SK-N-MC	brain:	n/a
6	chr6:150185369-150185419	RPTEC	kidney:	n/a
7	chr6:150183531-150183581	NHDF-neo	bronchial:	n/a
8	chr6:150184969-150185019	PrEC	prostate:	n/a
9	chr6:150183516-150183566	K562	blood:	n/a
10	chr6:150185198-150185248	NB4	blood:	n/a
11	chr6:150184969-150185019	MCF10A-Er-Src	breast:	n/a
12	chr6:150185809-150185859	GM12891	blood:	n/a
13	chr6:150185501-150185551	K562	blood:	n/a
14	chr6:150185632-150185682	RPTEC	kidney:	n/a
15	chr6:150184969-150185019	HCT-116	colon:	n/a
16	chr6:150183516-150183566	HAEpiC	amniotic membrane:	n/a
17	chr6:150183531-150183581	AG10803	skin:	n/a
18	chr6:150185501-150185551	NT2-D1	testis:	n/a
19	chr6:150184916-150184966	HCM	heart:	n/a
20	chr6:150184138-150184188	NHDF-neo	bronchial:	n/a
21	chr6:150185488-150185538	SK-N-SH	brain:	n/a
22	chr6:150185501-150185551	AG10803	skin:	n/a
23	chr6:150184138-150184188	HCT-116	colon:	n/a
24	chr6:150185499-150185549	NT2-D1	testis:	n/a
25	chr6:150185632-150185682	MCF10A-Er-Src	breast:	n/a
26	chr6:150184138-150184188	AG04450	lung:	fetal
27	chr6:150185499-150185549	GM06990	blood:	n/a
28	chr6:150185198-150185248	PANC-1	pancreas:	n/a
29	chr6:150184138-150184188	U87	brain:	n/a
30	chr6:150185809-150185859	LNCaP	prostate:	n/a
31	chr6:150185501-150185551	ECC-1	luminal epithelium:	n/a
32	chr6:150185501-150185551	HCM	heart:	n/a
33	chr6:150184969-150185019	HRPEpiC	eye:	n/a
34	chr6:150184916-150184966	BJ	skin:	n/a
35	chr6:150185809-150185859	AG10803	skin:	n/a
36	chr6:150185488-150185538	NT2-D1	testis:	n/a
37	chr6:150185854-150185904	GM06990	blood:	n/a
38	chr6:150185198-150185248	Caco-2	colon:	n/a
39	chr6:150185854-150185904	SKMC	muscle:	n/a
40	chr6:150183516-150183566	HIPEpiC	eye:	n/a
41	chr6:150185632-150185682	HCM	heart:	n/a
42	chr6:150185595-150185645	HCT-116	colon:	n/a
43	chr6:150185369-150185419	NH-A	brain:	n/a
44	chr6:150183516-150183566	A549	lung:	n/a
45	chr6:150185488-150185538	AG04449	skin:	fetal
46	chr6:150184345-150184395	MCF-7	breast:	n/a
47	chr6:150185499-150185549	K562	blood:	n/a
48	chr6:150185595-150185645	T-47D	breast:	n/a
49	chr6:150185499-150185549	BE2_C	brain:	n/a
50	chr6:150185488-150185538	HRCEpiC	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:149967481..149969834-chr6:150184237..150185789,2	K562	blood:
2	chr6:150181490..150187274-chr6:150243970..150248410,8	MCF-7	breast:
3	chr6:150183161..150188305-chr6:150206346..150214162,9	MCF-7	breast:
4	chr12:7053047..7053870-chr6:150185072..150185791,2	Hela-S3	cervix:
5	chr6:150037075..150038991-chr6:150181496..150184249,2	K562	blood:
6	chr6:150037040..150038886-chr6:150185486..150187035,2	K562	blood:
7	chr6:150156036..150158963-chr6:150184147..150187311,3	MCF-7	breast:
8	chr6:149865631..149868201-chr6:150184694..150186592,2	MCF-7	breast:
9	chr6:150185187..150186828-chr6:150215109..150217579,2	MCF-7	breast:
10	chr6:150183832..150186232-chr6:150215270..150224001,9	MCF-7	breast:
11	chr6:150036146..150038991-chr6:150182749..150185016,3	K562	blood:
12	chr6:150184661..150189239-chr6:150198084..150201371,4	MCF-7	breast:
13	chr6:150065257..150067789-chr6:150184620..150186500,2	K562	blood:
14	chr6:150067770..150069561-chr6:150184088..150185718,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAET1E-2	chr6:150184027-150184273	expReg_chr6_11262_-
2	lnc-ULBP2-3	chr6:150185338-150185480	NONHSAT115516

No data

Variant related genes	Relation type
ENSG00000268592	TF binding region
LRP11	TF binding region
ENSG00000268592	CpG island
LRP11	CpG island
ENSG00000223701	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000131013	chromatin interactions
ENSG00000131023	chromatin interactions
ENSG00000164520	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000217733	chromatin interactions
ENSG00000203722	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000186625	chromatin interactions
ENSG00000272173	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550793044	chr6:150183518-150183519	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs183285633	chr6:150183522-150183523	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs570802222	chr6:150183576-150183577	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs9371502	chr6:150183603-150183604	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553186265	chr6:150183676-150183677	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs375619712	chr6:150183686-150183687	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs201883603	chr6:150183707-150183708	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs200222844	chr6:150183711-150183712	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs369463509	chr6:150183713-150183714	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs67569936	chr6:150183714-150183715	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs10553273	chr6:150183732-150183733	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs9478192	chr6:150183737-150183738	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs188010639	chr6:150183759-150183760	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs554670765	chr6:150183809-150183810	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs574588800	chr6:150183828-150183829	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs543646466	chr6:150183860-150183861	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs190715940	chr6:150183867-150183868	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs370912965	chr6:150183877-150183878	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs55932834	chr6:150183900-150183901	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs374138673	chr6:150183917-150183918	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs183009853	chr6:150183968-150183969	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs9371504	chr6:150184080-150184081	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs9371505	chr6:150184148-150184149	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs374494660	chr6:150184163-150184164	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
25	rs146962172	chr6:150184208-150184209	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
26	rs528110679	chr6:150184218-150184219	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs541827577	chr6:150184234-150184235	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
28	rs149464398	chr6:150184256-150184257	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
29	rs371338711	chr6:150184283-150184284	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs530613959	chr6:150184358-150184359	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs550654800	chr6:150184390-150184391	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs570558607	chr6:150184465-150184466	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs374706154	chr6:150184503-150184504	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs143869691	chr6:150184601-150184602	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs546611868	chr6:150184611-150184612	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs571328083	chr6:150184705-150184706	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs187967019	chr6:150184722-150184723	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs534756146	chr6:150184866-150184867	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs548167870	chr6:150184876-150184877	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs9322225	chr6:150184882-150184883	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs17854253	chr6:150184887-150184888	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs537149119	chr6:150184940-150184941	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs192815318	chr6:150184947-150184948	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs112177925	chr6:150185024-150185025	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs371377255	chr6:150185031-150185032	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs540009536	chr6:150185035-150185036	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs553420799	chr6:150185186-150185187	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs573480996	chr6:150185206-150185207	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs139821496	chr6:150185216-150185217	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs541888743	chr6:150185258-150185259	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150173000-150184200	Weak transcription	Aorta	Aorta
2	chr6:150178600-150184000	Weak transcription	Psoas Muscle	Psoas
3	chr6:150180600-150183600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:150180600-150183600	Enhancers	Gastric	stomach
5	chr6:150180600-150184200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:150181200-150183600	Enhancers	Esophagus	oesophagus
7	chr6:150181200-150183800	Enhancers	Fetal Muscle Leg	muscle
8	chr6:150181200-150183800	Enhancers	Placenta	Placenta
9	chr6:150181200-150183800	Enhancers	Pancreas	Pancrea
10	chr6:150181200-150183800	Flanking Active TSS	Hela-S3	cervix
11	chr6:150181200-150184000	Enhancers	Liver	Liver
12	chr6:150181800-150183800	Enhancers	Adipose Nuclei	Adipose
13	chr6:150181800-150183800	Enhancers	Brain Germinal Matrix	brain
14	chr6:150182000-150184000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr6:150182000-150184000	Enhancers	Left Ventricle	heart
16	chr6:150182000-150184000	Enhancers	Stomach Mucosa	stomach
17	chr6:150182000-150186200	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr6:150182200-150183600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr6:150182200-150184200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:150182200-150184200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:150182400-150183600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:150182400-150183600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr6:150182400-150183800	Flanking Active TSS	Osteobl	bone
24	chr6:150182400-150184200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:150182600-150183800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:150182600-150183800	Enhancers	Fetal Muscle Trunk	muscle
27	chr6:150182600-150184000	Enhancers	Dnd41	blood
28	chr6:150182800-150183800	Flanking Active TSS	HepG2	liver
29	chr6:150183000-150183600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:150183000-150183600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:150183000-150183600	Flanking Active TSS	Brain Angular Gyrus	brain
32	chr6:150183000-150183600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr6:150183000-150183600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr6:150183000-150183800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:150183000-150184000	Enhancers	Brain Substantia Nigra	brain
36	chr6:150183000-150184000	Enhancers	Fetal Brain Male	brain
37	chr6:150183000-150184000	Enhancers	Fetal Kidney	kidney
38	chr6:150183200-150183600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
39	chr6:150183200-150183600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:150183200-150183600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:150183200-150183600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:150183200-150183600	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr6:150183200-150183600	Transcr. at gene 5' and 3'	Brain Dorsolateral Prefrontal Cortex	brain
44	chr6:150183200-150183600	Enhancers	Colon Smooth Muscle	Colon
45	chr6:150183200-150183600	Enhancers	HSMM	muscle
46	chr6:150183200-150183600	Transcr. at gene 5' and 3'	NHLF	lung
47	chr6:150183200-150183800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr6:150183200-150183800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:150183200-150183800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:150183200-150183800	Enhancers	Colonic Mucosa	Colon

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