Variant report

Variant	esv3331798
Chromosome Location	chr7:127670766-127673564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:856)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:127672788-127673046	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:127671979-127672314	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:127670863-127671041	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:127672060-127672304	GM12878	blood:	n/a	n/a
5	CCNT2	chr7:127671978-127672310	K562	blood:	n/a	n/a
6	CHD1	chr7:127671420-127671423	GM12878	blood:	n/a	n/a
7	CHD1	chr7:127671127-127671606	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr7:127670862-127670865	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr7:127671433-127671537	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:127672022-127672206	H1-hESC	embryonic stem cell:	n/a	chr7:127672074-127672084
11	CREB1	chr7:127672482-127672900	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:127672000-127672150	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr7:127672080-127672230	RPTEC	kidney:	n/a	n/a
14	CTCF	chr7:127672060-127672210	AG09319	gingival:	n/a	n/a
15	CTCF	chr7:127671980-127672130	GM12869	blood:	n/a	n/a
16	CTCF	chr7:127672178-127672240	GM19239	blood:	n/a	n/a
17	CTCF	chr7:127671420-127671570	GM12867	blood:	n/a	n/a
18	CTCF	chr7:127672040-127672190	GM12871	blood:	n/a	n/a
19	CTCF	chr7:127671980-127672130	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr7:127672040-127672190	GM12864	blood:	n/a	n/a
21	CTCF	chr7:127672020-127672170	GM12871	blood:	n/a	n/a
22	CTCF	chr7:127671420-127671570	HAc	cerebellar:	n/a	n/a
23	CTCF	chr7:127671360-127671510	AG09319	gingival:	n/a	n/a
24	CTCF	chr7:127672060-127672210	SAEC	small airway:	n/a	n/a
25	CTCF	chr7:127672018-127672190	Gliobla	brain:	n/a	n/a
26	CTCF	chr7:127671920-127672070	GM12874	blood:	n/a	n/a
27	CTCF	chr7:127672002-127672194	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr7:127671410-127671530	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:127671418-127671537	ProgFib	skin:	n/a	n/a
30	CTCF	chr7:127671379-127671546	GM12892	blood:	n/a	n/a
31	CTCF	chr7:127671380-127671530	HMEC	breast:	n/a	n/a
32	CTCF	chr7:127672043-127672185	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:127671320-127671470	GM12871	blood:	n/a	n/a
34	CTCF	chr7:127671420-127671570	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr7:127671373-127671504	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr7:127671340-127671490	AG04450	lung:	n/a	n/a
37	CTCF	chr7:127672060-127672210	HPF	lung:	n/a	n/a
38	CTCF	chr7:127672020-127672170	NHLF	lung:	n/a	n/a
39	CTCF	chr7:127671940-127672090	GM12865	blood:	n/a	n/a
40	CTCF	chr7:127671954-127672239	Fibrobl	skin:	n/a	n/a
41	CTCF	chr7:127671360-127671510	GM12866	blood:	n/a	n/a
42	CTCF	chr7:127672184-127672186	GM13977	blood:	n/a	n/a
43	CTCF	chr7:127671400-127671506	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:127671436-127671440	GM20000	blood:	n/a	n/a
45	CTCF	chr7:127672000-127672150	HEK293	kidney:	n/a	n/a
46	CTCF	chr7:127672040-127672190	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:127672020-127672170	GM12874	blood:	n/a	n/a
48	CTCF	chr7:127671360-127671510	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr7:127672065-127672211	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr7:127671320-127671470	WERI-Rb-1	eye:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127672235-127672285	AG04450	lung:	fetal
2	chr7:127672458-127672508	HL-60	blood:	n/a
3	chr7:127672235-127672285	AG04450	lung:	fetal
4	chr7:127672458-127672508	HL-60	blood:	n/a
5	chr7:127671044-127671094	HEEpiC	esophagus:	n/a
6	chr7:127672152-127672202	NT2-D1	testis:	n/a
7	chr7:127672473-127672523	AG04450	lung:	fetal
8	chr7:127672235-127672285	HNPCEpiC	eye:	n/a
9	chr7:127672564-127672614	GM19239	blood:	n/a
10	chr7:127671017-127671067	NT2-D1	testis:	n/a
11	chr7:127671193-127671243	MCF-7	breast:	n/a
12	chr7:127671193-127671243	AG09309	skin:	n/a
13	chr7:127671195-127671245	MCF10A-Er-Src	breast:	n/a
14	chr7:127671195-127671245	IMR90	lung:	fetal
15	chr7:127672152-127672202	SK-N-SH_RA	brain:	n/a
16	chr7:127672658-127672708	AG10803	skin:	n/a
17	chr7:127672658-127672708	H1-hESC	embryonic stem cell:	embryo
18	chr7:127671044-127671094	HepG2	liver:	n/a
19	chr7:127672152-127672202	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:127672564-127672614	AG09309	skin:	n/a
21	chr7:127671044-127671094	Hela-S3	cervix:	n/a
22	chr7:127671033-127671083	HCM	heart:	n/a
23	chr7:127671033-127671083	AG09309	skin:	n/a
24	chr7:127672169-127672219	GM12878	blood:	n/a
25	chr7:127671195-127671245	PFSK-1	brain:	n/a
26	chr7:127672169-127672219	PANC-1	pancreas:	n/a
27	chr7:127672658-127672708	GM06990	blood:	n/a
28	chr7:127671033-127671083	A549	lung:	n/a
29	chr7:127671044-127671094	SK-N-SH_RA	brain:	n/a
30	chr7:127671195-127671245	HNPCEpiC	eye:	n/a
31	chr7:127670993-127671043	HCM	heart:	n/a
32	chr7:127672152-127672202	GM12891	blood:	n/a
33	chr7:127672235-127672285	HEEpiC	esophagus:	n/a
34	chr7:127672473-127672523	HCPEpiC	choroid plexus:	n/a
35	chr7:127671044-127671094	MCF-7	breast:	n/a
36	chr7:127672235-127672285	HIPEpiC	eye:	n/a
37	chr7:127672473-127672523	HCF	heart:	n/a
38	chr7:127671017-127671067	K562	blood:	n/a
39	chr7:127671044-127671094	HCF	heart:	n/a
40	chr7:127672235-127672285	SK-N-MC	brain:	n/a
41	chr7:127672152-127672202	K562	blood:	n/a
42	chr7:127672152-127672202	Hepatocyte	liver:	n/a
43	chr7:127672564-127672614	Hela-S3	cervix:	n/a
44	chr7:127670993-127671043	Hela-S3	cervix:	n/a
45	chr7:127671017-127671067	SK-N-SH_RA	brain:	n/a
46	chr7:127673038-127673088	HRE	kidney:	n/a
47	chr7:127671017-127671067	HNPCEpiC	eye:	n/a
48	chr7:127671017-127671067	GM06990	blood:	n/a
49	chr7:127672169-127672219	HCF	heart:	n/a
50	chr7:127672564-127672614	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:127672744..127674638-chr7:127845082..127846622,2	K562	blood:
2	chr7:127672187..127674051-chr7:127688300..127690712,2	K562	blood:
3	chr7:127673149..127675504-chr7:127681754..127684227,2	MCF-7	breast:
4	chr7:127227216..127230211-chr7:127672180..127674348,2	MCF-7	breast:
5	chr7:127666110..127669340-chr7:127673259..127677722,5	K562	blood:
6	chr7:127671143..127673584-chr7:127727975..127729974,2	MCF-7	breast:
7	chr7:127670290..127672426-chr7:127847694..127849550,2	MCF-7	breast:
8	chr7:127669395..127671231-chr7:127673315..127675845,3	K562	blood:

No data

Variant related genes	Relation type
LRRC4	TF binding region
LRRC4	CpG island
ENSG00000207705	chromatin interactions
ENSG00000128594	chromatin interactions
ENSG00000197157	chromatin interactions
ENSG00000004059	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527541384	chr7:127670786-127670787	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs112859413	chr7:127670788-127670789	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112291805	chr7:127670789-127670790	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138180193	chr7:127670810-127670811	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149139797	chr7:127670813-127670814	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549286961	chr7:127670814-127670815	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568511382	chr7:127670839-127670840	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559634295	chr7:127670898-127670899	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530299854	chr7:127670973-127670974	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542207382	chr7:127671014-127671015	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547734045	chr7:127671026-127671027	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531074627	chr7:127671033-127671034	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115852530	chr7:127671050-127671051	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571447491	chr7:127671054-127671055	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532329508	chr7:127671078-127671079	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs143219003	chr7:127671140-127671141	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566002579	chr7:127671146-127671147	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs536504866	chr7:127671174-127671175	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554558750	chr7:127671243-127671244	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs111614365	chr7:127671266-127671267	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537199340	chr7:127671294-127671295	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs558349372	chr7:127671428-127671429	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577058632	chr7:127671458-127671459	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs79520962	chr7:127671511-127671512	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs183631649	chr7:127671537-127671538	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs76383325	chr7:127671588-127671589	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs542147200	chr7:127671610-127671611	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs552289897	chr7:127671786-127671787	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs563748905	chr7:127671806-127671807	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs564375276	chr7:127671837-127671838	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs929715	chr7:127671842-127671843	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs929716	chr7:127671846-127671847	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564588464	chr7:127671851-127671852	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs528569657	chr7:127671982-127671983	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs547617252	chr7:127671997-127671998	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs559548243	chr7:127672012-127672013	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs530047069	chr7:127672029-127672030	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs113331226	chr7:127672035-127672036	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs548186999	chr7:127672074-127672075	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs142220343	chr7:127672115-127672116	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs186143191	chr7:127672125-127672126	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs552121097	chr7:127672204-127672205	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs570212844	chr7:127672230-127672231	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534372560	chr7:127672249-127672250	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568863560	chr7:127672273-127672274	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs553188519	chr7:127672284-127672285	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs574688951	chr7:127672287-127672288	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs536173559	chr7:127672288-127672289	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs557354304	chr7:127672361-127672362	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs3735635	chr7:127672377-127672378	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Myxofibrosarcoma	20639860	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127644800-127670800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr7:127645000-127684000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr7:127663200-127671200	Weak transcription	NHLF	lung
4	chr7:127663200-127671400	Weak transcription	NHDF-Ad	bronchial
5	chr7:127663600-127670800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:127666000-127670800	Weak transcription	HMEC	breast
7	chr7:127666000-127670800	Weak transcription	Osteobl	bone
8	chr7:127666200-127672600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:127666800-127670800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:127668200-127670800	Weak transcription	HSMMtube	muscle
11	chr7:127668200-127672200	Weak transcription	Fetal Heart	heart
12	chr7:127668600-127670800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:127668800-127671000	ZNF genes & repeats	K562	blood
14	chr7:127669000-127670800	Strong transcription	HepG2	liver
15	chr7:127669400-127671200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:127669400-127671400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr7:127669400-127726600	Weak transcription	Hela-S3	cervix
18	chr7:127669600-127670800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr7:127669600-127671200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:127669600-127671200	Enhancers	Liver	Liver
21	chr7:127669600-127673200	Active TSS	Brain Cingulate Gyrus	brain
22	chr7:127669600-127718200	Weak transcription	A549	lung
23	chr7:127669800-127670800	Weak transcription	Aorta	Aorta
24	chr7:127669800-127671200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:127670000-127670800	Weak transcription	Primary T cells from cord blood	blood
26	chr7:127670000-127670800	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr7:127670000-127670800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:127670000-127670800	Weak transcription	Pancreas	Pancrea
29	chr7:127670000-127671200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr7:127670000-127673000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:127670000-127673200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
32	chr7:127670200-127670800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
33	chr7:127670200-127670800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:127670200-127670800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr7:127670200-127670800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr7:127670200-127670800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:127670200-127670800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:127670200-127670800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr7:127670200-127670800	Transcr. at gene 5' and 3'	HSMM	muscle
40	chr7:127670200-127671000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr7:127670200-127671000	Enhancers	Ovary	ovary
42	chr7:127670200-127671000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
43	chr7:127670200-127673000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:127670400-127670800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:127670400-127670800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:127670400-127670800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:127670400-127670800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr7:127670400-127670800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:127670400-127670800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:127670400-127670800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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