Variant report

Variant	esv3403555
Chromosome Location	chr11:67187476-67189674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:429)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:67188448-67188718	K562	blood:	n/a	n/a
2	BACH1	chr11:67187790-67187821	K562	blood:	n/a	n/a
3	BACH1	chr11:67188387-67188748	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr11:67187937-67188334	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:67188258-67188614	HepG2	liver:	n/a	chr11:67188345-67188361
6	BHLHE40	chr11:67188399-67188616	K562	blood:	n/a	n/a
7	BHLHE40	chr11:67188067-67188131	K562	blood:	n/a	n/a
8	BHLHE40	chr11:67188429-67188611	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:67188009-67188193	GM12878	blood:	n/a	n/a
10	BRCA1	chr11:67188731-67188974	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr11:67188439-67188784	K562	blood:	n/a	n/a
12	CCNT2	chr11:67188066-67188877	K562	blood:	n/a	n/a
13	CEBPD	chr11:67188359-67188608	HepG2	liver:	n/a	n/a
14	CHD1	chr11:67188358-67188557	GM12878	blood:	n/a	chr11:67188391-67188401
15	CHD2	chr11:67188578-67188798	GM12878	blood:	n/a	n/a
16	CHD2	chr11:67188418-67189043	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr11:67188532-67188534	K562	blood:	n/a	n/a
18	CHD2	chr11:67188743-67188905	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr11:67188260-67188936	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr11:67188359-67188879	K562	blood:	n/a	n/a
21	CREB1	chr11:67188052-67189099	A549	lung:	n/a	n/a
22	CTCF	chr11:67188547-67188570	GM19238	blood:	n/a	n/a
23	CTCF	chr11:67188114-67188227	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr11:67188081-67188232	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:67189063-67189155	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:67188880-67189030	Caco-2	colon:	n/a	n/a
27	CTCF	chr11:67188569-67188613	K562	blood:	n/a	n/a
28	CTCF	chr11:67188017-67188225	GM12891	blood:	n/a	n/a
29	CTCF	chr11:67188040-67188190	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr11:67188020-67188170	GM12875	blood:	n/a	n/a
31	CTCF	chr11:67189060-67189210	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr11:67188099-67188226	Fibrobl	skin:	n/a	n/a
33	CTCF	chr11:67188089-67188209	GM19240	blood:	n/a	n/a
34	CTCF	chr11:67188520-67188670	AG04449	skin:	n/a	n/a
35	CTCF	chr11:67188552-67188658	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr11:67188094-67188195	NHEK	skin:	n/a	n/a
37	CTCF	chr11:67189069-67189175	LNCaP	prostate:	n/a	n/a
38	CTCF	chr11:67188980-67189130	NHEK	skin:	n/a	n/a
39	CTCF	chr11:67188070-67188206	GM19238	blood:	n/a	n/a
40	CTCF	chr11:67188200-67188350	Caco-2	colon:	n/a	n/a
41	CTCF	chr11:67188041-67188245	GM19239	blood:	n/a	n/a
42	CTCF	chr11:67189050-67189185	NHEK	skin:	n/a	n/a
43	CTCF	chr11:67188060-67188210	GM12866	blood:	n/a	n/a
44	CTCF	chr11:67189021-67189204	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr11:67189062-67189128	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr11:67188520-67188670	GM12869	blood:	n/a	n/a
47	CTCF	chr11:67189040-67189190	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:67188531-67188823	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr11:67188040-67188190	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr11:67188040-67188190	GM12874	blood:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67188491-67188541	U87	brain:	n/a
2	chr11:67188673-67188723	T-47D	breast:	n/a
3	chr11:67188491-67188541	U87	brain:	n/a
4	chr11:67188673-67188723	T-47D	breast:	n/a
5	chr11:67188673-67188723	Hepatocyte	liver:	n/a
6	chr11:67189121-67189171	CMK	blood:	n/a
7	chr11:67188192-67188242	MCF10A-Er-Src	breast:	n/a
8	chr11:67188521-67188571	LNCaP	prostate:	n/a
9	chr11:67188673-67188723	GM12892	blood:	n/a
10	chr11:67188673-67188723	SKMC	muscle:	n/a
11	chr11:67188673-67188723	GM12891	blood:	n/a
12	chr11:67188696-67188746	ECC-1	luminal epithelium:	n/a
13	chr11:67188673-67188723	HCF	heart:	n/a
14	chr11:67188521-67188571	HRPEpiC	eye:	n/a
15	chr11:67188871-67188921	SKMC	muscle:	n/a
16	chr11:67189121-67189171	HUVEC	blood vessel:	n/a
17	chr11:67189121-67189171	ProgFib	skin:	n/a
18	chr11:67188696-67188746	Hepatocyte	liver:	n/a
19	chr11:67188871-67188921	AG09309	skin:	n/a
20	chr11:67188192-67188242	AG09319	gingival:	n/a
21	chr11:67188521-67188571	PANC-1	pancreas:	n/a
22	chr11:67188491-67188541	AG04449	skin:	fetal
23	chr11:67189121-67189171	SAEC	small airway:	n/a
24	chr11:67189121-67189171	NHBE	bronchial:	n/a
25	chr11:67188696-67188746	HepG2	liver:	n/a
26	chr11:67188192-67188242	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:67188521-67188571	ProgFib	skin:	n/a
28	chr11:67188521-67188571	GM19239	blood:	n/a
29	chr11:67188521-67188571	MCF10A-Er-Src	breast:	n/a
30	chr11:67188871-67188921	AG04449	skin:	fetal
31	chr11:67189121-67189171	T-47D	breast:	n/a
32	chr11:67188521-67188571	SK-N-MC	brain:	n/a
33	chr11:67188871-67188921	HUVEC	blood vessel:	n/a
34	chr11:67189121-67189171	NT2-D1	testis:	n/a
35	chr11:67188871-67188921	ECC-1	luminal epithelium:	n/a
36	chr11:67188871-67188921	PFSK-1	brain:	n/a
37	chr11:67188673-67188723	GM19239	blood:	n/a
38	chr11:67189121-67189171	HCF	heart:	n/a
39	chr11:67188192-67188242	HAEpiC	amniotic membrane:	n/a
40	chr11:67188871-67188921	NT2-D1	testis:	n/a
41	chr11:67188491-67188541	SK-N-SH_RA	brain:	n/a
42	chr11:67188673-67188723	AoSMC	blood vessel:	n/a
43	chr11:67188673-67188723	GM12878	blood:	n/a
44	chr11:67188521-67188571	HCM	heart:	n/a
45	chr11:67188871-67188921	SK-N-SH	brain:	n/a
46	chr11:67188521-67188571	HMEC	breast:	n/a
47	chr11:67188521-67188571	HepG2	liver:	n/a
48	chr11:67188521-67188571	AG09319	gingival:	n/a
49	chr11:67188871-67188921	GM12891	blood:	n/a
50	chr11:67188673-67188723	AG09309	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67186666..67191064-chr11:67273296..67275634,4	K562	blood:
2	chr11:67186666..67189529-chr11:67272076..67275550,4	K562	blood:
3	chr11:67168977..67169771-chr11:67188130..67189217,5	K562	blood:
4	chr11:67187671..67190437-chr11:67260669..67262502,2	MCF-7	breast:
5	chr11:67140365..67142235-chr11:67187974..67189991,2	K562	blood:
6	chr11:67185544..67187965-chr11:67270918..67273442,2	MCF-7	breast:
7	chr11:67187544..67192614-chr11:67201349..67205044,6	K562	blood:
8	chr11:67187290..67189722-chr11:67250373..67251986,2	K562	blood:
9	chr11:67185700..67187766-chr11:67250423..67251941,2	K562	blood:
10	chr11:67188329..67190078-chr11:67395497..67397471,2	K562	blood:
11	chr11:67147040..67148988-chr11:67186808..67188399,2	K562	blood:
12	chr11:67185549..67189385-chr11:67208691..67212904,6	K562	blood:
13	chr11:67123845..67125865-chr11:67186294..67189193,2	K562	blood:
14	chr11:67119033..67122416-chr11:67186034..67189246,4	K562	blood:
15	chr11:67186236..67188568-chr11:67242107..67244785,2	MCF-7	breast:
16	chr11:67138903..67140672-chr11:67189332..67192243,2	K562	blood:
17	chr11:67187592..67190127-chr11:67230614..67234165,3	K562	blood:
18	chr11:67117328..67119147-chr11:67188918..67191824,2	K562	blood:
19	chr11:67182567..67190511-chr11:67270739..67276166,13	MCF-7	breast:

No data

Variant related genes	Relation type
PPP1CA	TF binding region
CARNS1	TF binding region
PPP1CA	CpG island
CARNS1	CpG island
ENSG00000255949	chromatin interactions
ENSG00000110711	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000175482	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000172725	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000172531	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560649410	chr11:67187497-67187498	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs527865429	chr11:67187512-67187513	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs188621566	chr11:67187519-67187520	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs561620694	chr11:67187523-67187524	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs564437566	chr11:67187525-67187526	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs148588805	chr11:67187560-67187561	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs61891596	chr11:67187561-67187562	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs531920095	chr11:67187567-67187568	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs35876769	chr11:67187586-67187587	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568711309	chr11:67187635-67187636	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs536267625	chr11:67187686-67187687	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs78932458	chr11:67187778-67187779	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs370766136	chr11:67187799-67187800	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs566598683	chr11:67187870-67187871	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs7116138	chr11:67187931-67187932	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs533956278	chr11:67187968-67187969	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs180979047	chr11:67187977-67187978	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs577201431	chr11:67187978-67187979	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs538098256	chr11:67187986-67187987	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs556426905	chr11:67187994-67187995	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs374662414	chr11:67188027-67188028	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs12786101	chr11:67188111-67188112	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs12787600	chr11:67188112-67188113	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs537788289	chr11:67188145-67188146	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs112037976	chr11:67188230-67188231	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs542241181	chr11:67188347-67188348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs560360709	chr11:67188427-67188428	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs528083996	chr11:67188446-67188447	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs77472930	chr11:67188466-67188467	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs545975688	chr11:67188496-67188497	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs564297287	chr11:67188538-67188539	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs185303034	chr11:67188549-67188550	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs12277001	chr11:67188594-67188595	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs562422049	chr11:67188606-67188607	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs529644285	chr11:67188619-67188620	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs528939487	chr11:67188666-67188667	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs548198385	chr11:67188671-67188672	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs192099699	chr11:67188745-67188746	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs533915674	chr11:67188773-67188774	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs552311284	chr11:67188778-67188779	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs368105354	chr11:67188829-67188830	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs562474055	chr11:67188851-67188852	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs12290164	chr11:67188860-67188861	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs183894944	chr11:67188917-67188918	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs143587522	chr11:67188922-67188923	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs567520568	chr11:67188965-67188966	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs535477487	chr11:67188994-67188995	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs533698837	chr11:67189055-67189056	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs148067057	chr11:67189261-67189262	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs566770786	chr11:67189323-67189324	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67182600-67187600	Enhancers	Rectal Mucosa Donor 29	rectum
2	chr11:67182600-67188000	Enhancers	Spleen	Spleen
3	chr11:67183000-67187600	Enhancers	Fetal Thymus	thymus
4	chr11:67183000-67187600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:67183000-67187600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr11:67183000-67187800	Enhancers	Primary hematopoietic stem cells	blood
7	chr11:67183000-67188000	Enhancers	Esophagus	oesophagus
8	chr11:67183000-67188000	Enhancers	Fetal Lung	lung
9	chr11:67183200-67187600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:67183200-67188000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:67183400-67187800	Enhancers	Right Ventricle	heart
12	chr11:67183400-67188000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr11:67183400-67188000	Enhancers	Left Ventricle	heart
14	chr11:67183400-67188200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr11:67183400-67188200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr11:67183600-67187600	Weak transcription	Osteobl	bone
17	chr11:67183600-67187800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:67183600-67188000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:67183600-67188000	Enhancers	Right Atrium	heart
20	chr11:67183600-67188200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
21	chr11:67183800-67187800	Weak transcription	NHDF-Ad	bronchial
22	chr11:67183800-67188000	Enhancers	Gastric	stomach
23	chr11:67184000-67187800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr11:67184200-67187600	Weak transcription	Aorta	Aorta
25	chr11:67184200-67188200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
26	chr11:67184200-67188800	Enhancers	Placenta	Placenta
27	chr11:67184400-67187600	Weak transcription	Colon Smooth Muscle	Colon
28	chr11:67184400-67187800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:67184400-67188000	Enhancers	Psoas Muscle	Psoas
30	chr11:67184600-67187600	Enhancers	Primary B cells from cord blood	blood
31	chr11:67184600-67187600	Weak transcription	Fetal Kidney	kidney
32	chr11:67184600-67187800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:67184600-67187800	Enhancers	Brain Angular Gyrus	brain
34	chr11:67184800-67187600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:67184800-67187800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr11:67184800-67188000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:67184800-67188200	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr11:67185000-67187600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:67185000-67187800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:67185000-67187800	Enhancers	Brain Anterior Caudate	brain
41	chr11:67185200-67187800	Enhancers	Liver	Liver
42	chr11:67185400-67187800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:67185600-67187600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr11:67185600-67187800	Enhancers	Brain Substantia Nigra	brain
45	chr11:67185600-67188000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr11:67185600-67188600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr11:67185800-67187600	Enhancers	Colonic Mucosa	Colon
48	chr11:67186000-67187800	Enhancers	Adipose Nuclei	Adipose
49	chr11:67186000-67188000	Enhancers	HMEC	breast
50	chr11:67186000-67188200	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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