Variant report

Variant	esv3440198
Chromosome Location	chr7:106684366-106686514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:106686119-106686128	K562	blood:	n/a	n/a
2	ARID3A	chr7:106686436-106687016	K562	blood:	n/a	n/a
3	ATF3	chr7:106684939-106685047	GM12878	blood:	n/a	n/a
4	ATF3	chr7:106684767-106685193	K562	blood:	n/a	n/a
5	ATF3	chr7:106684720-106685204	K562	blood:	n/a	n/a
6	ATF3	chr7:106684819-106685165	HepG2	liver:	n/a	n/a
7	ATF3	chr7:106684830-106685195	K562	blood:	n/a	n/a
8	ATF3	chr7:106684878-106685106	GM12878	blood:	n/a	n/a
9	ATF3	chr7:106684783-106685185	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr7:106684725-106685549	K562	blood:	n/a	chr7:106685276-106685289 chr7:106685273-106685286
11	BHLHE40	chr7:106684797-106685153	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:106684938-106685051	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:106684591-106685557	K562	blood:	n/a	chr7:106685276-106685292 chr7:106685268-106685284 chr7:106685323-106685339
14	CBX3	chr7:106684434-106685168	K562	blood:	n/a	n/a
15	CBX3	chr7:106685194-106686254	K562	blood:	n/a	n/a
16	CCNT2	chr7:106684685-106685697	K562	blood:	n/a	n/a
17	CCNT2	chr7:106686463-106686761	K562	blood:	n/a	n/a
18	CEBPB	chr7:106686441-106686916	IMR90	lung:	n/a	chr7:106686624-106686635
19	CEBPB	chr7:106686443-106686871	K562	blood:	n/a	chr7:106686624-106686635
20	CEBPB	chr7:106685906-106687126	K562	blood:	n/a	chr7:106686108-106686116 chr7:106686624-106686635
21	CEBPB	chr7:106686416-106686948	MCF-7	breast:	n/a	chr7:106686624-106686635
22	CEBPB	chr7:106686458-106686790	K562	blood:	n/a	chr7:106686624-106686635
23	CEBPD	chr7:106684892-106685163	HepG2	liver:	n/a	n/a
24	CHD2	chr7:106685481-106685483	K562	blood:	n/a	n/a
25	CHD2	chr7:106684778-106685150	K562	blood:	n/a	n/a
26	CREB1	chr7:106684730-106685322	A549	lung:	n/a	n/a
27	CTBP2	chr7:106684634-106685410	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:106685820-106685970	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr7:106684914-106685177	MCF-7	breast:	n/a	chr7:106685133-106685146 chr7:106684976-106684989
30	CTCF	chr7:106684940-106685090	GM12874	blood:	n/a	chr7:106684976-106684989
31	CTCF	chr7:106684860-106685097	SK-N-SH_RA	brain:	n/a	chr7:106684861-106684874 chr7:106684976-106684989
32	CTCF	chr7:106684953-106685062	GM12878	blood:	n/a	chr7:106684976-106684989
33	CTCF	chr7:106685020-106685170	HBMEC	blood vessel:	n/a	chr7:106685133-106685146
34	CTCF	chr7:106684866-106685128	Fibrobl	skin:	n/a	chr7:106684976-106684989
35	CTCF	chr7:106684960-106685110	GM12875	blood:	n/a	chr7:106684976-106684989
36	CTCF	chr7:106685000-106685150	GM12866	blood:	n/a	chr7:106685133-106685146
37	CTCF	chr7:106684860-106685010	SAEC	small airway:	n/a	chr7:106684861-106684874 chr7:106684976-106684989
38	CTCF	chr7:106684960-106685110	GM12871	blood:	n/a	chr7:106684976-106684989
39	CTCF	chr7:106684926-106685102	ProgFib	skin:	n/a	chr7:106684976-106684989
40	CTCF	chr7:106684900-106685050	HCPEpiC	choroid plexus:	n/a	chr7:106684976-106684989
41	CTCF	chr7:106684860-106685010	GM12867	blood:	n/a	chr7:106684861-106684874 chr7:106684976-106684989
42	CTCF	chr7:106684940-106685090	GM12869	blood:	n/a	chr7:106684976-106684989
43	CTCF	chr7:106684956-106685063	GM19240	blood:	n/a	chr7:106684976-106684989
44	CTCF	chr7:106684900-106685050	AG04449	skin:	n/a	chr7:106684976-106684989
45	CTCF	chr7:106684999-106685043	NHEK	skin:	n/a	n/a
46	CTCF	chr7:106684940-106685090	GM12868	blood:	n/a	chr7:106684976-106684989
47	CTCF	chr7:106684902-106685133	MCF-7	breast:	n/a	chr7:106684976-106684989
48	CTCF	chr7:106684861-106685102	SK-N-SH_RA	brain:	n/a	chr7:106684861-106684874 chr7:106684976-106684989
49	CTCF	chr7:106684987-106685150	GM12878	blood:	n/a	chr7:106685133-106685146
50	CTCF	chr7:106684900-106685050	SK-N-SH_RA	brain:	n/a	chr7:106684976-106684989

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:106685015-106685065	NB4	blood:	n/a
2	chr7:106685015-106685065	NB4	blood:	n/a
3	chr7:106685033-106685083	Hela-S3	cervix:	n/a
4	chr7:106685023-106685073	H1-hESC	embryonic stem cell:	embryo
5	chr7:106685427-106685477	SK-N-SH	brain:	n/a
6	chr7:106685023-106685073	NHBE	bronchial:	n/a
7	chr7:106686041-106686091	HRE	kidney:	n/a
8	chr7:106684541-106684591	HL-60	blood:	n/a
9	chr7:106685023-106685073	AoSMC	blood vessel:	n/a
10	chr7:106685033-106685083	HIPEpiC	eye:	n/a
11	chr7:106686041-106686091	H1-hESC	embryonic stem cell:	embryo
12	chr7:106685977-106686027	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:106685977-106686027	Caco-2	colon:	n/a
14	chr7:106684814-106684864	H1-hESC	embryonic stem cell:	embryo
15	chr7:106685553-106685603	BE2_C	brain:	n/a
16	chr7:106686041-106686091	HL-60	blood:	n/a
17	chr7:106685021-106685071	NH-A	brain:	n/a
18	chr7:106685015-106685065	GM12891	blood:	n/a
19	chr7:106685021-106685071	Jurkat	blood:	n/a
20	chr7:106684814-106684864	SK-N-MC	brain:	n/a
21	chr7:106685023-106685073	CMK	blood:	n/a
22	chr7:106685023-106685073	SK-N-SH_RA	brain:	n/a
23	chr7:106685023-106685073	MCF10A-Er-Src	breast:	n/a
24	chr7:106685021-106685071	AoSMC	blood vessel:	n/a
25	chr7:106685021-106685071	HCM	heart:	n/a
26	chr7:106684541-106684591	NH-A	brain:	n/a
27	chr7:106684814-106684864	HRPEpiC	eye:	n/a
28	chr7:106685553-106685603	NH-A	brain:	n/a
29	chr7:106684814-106684864	NT2-D1	testis:	n/a
30	chr7:106684541-106684591	GM12878	blood:	n/a
31	chr7:106684814-106684864	HRE	kidney:	n/a
32	chr7:106685553-106685603	HRCEpiC	kidney:	n/a
33	chr7:106685023-106685073	PFSK-1	brain:	n/a
34	chr7:106685023-106685073	HMEC	breast:	n/a
35	chr7:106684814-106684864	PrEC	prostate:	n/a
36	chr7:106684541-106684591	Hepatocyte	liver:	n/a
37	chr7:106685977-106686027	Jurkat	blood:	n/a
38	chr7:106686041-106686091	HMEC	breast:	n/a
39	chr7:106685021-106685071	BJ	skin:	n/a
40	chr7:106686041-106686091	HRPEpiC	eye:	n/a
41	chr7:106685023-106685073	SKMC	muscle:	n/a
42	chr7:106686041-106686091	PrEC	prostate:	n/a
43	chr7:106684814-106684864	U87	brain:	n/a
44	chr7:106685553-106685603	HMEC	breast:	n/a
45	chr7:106685427-106685477	T-47D	breast:	n/a
46	chr7:106685033-106685083	Caco-2	colon:	n/a
47	chr7:106685023-106685073	AG04449	skin:	fetal
48	chr7:106686041-106686091	HRCEpiC	kidney:	n/a
49	chr7:106684814-106684864	Hela-S3	cervix:	n/a
50	chr7:106684814-106684864	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:106682746..106686911-chr7:106807556..106811745,9	K562	blood:
2	chr7:106685233..106687642-chr7:106786297..106788782,2	K562	blood:
3	chr7:106685168..106686791-chr7:107384430..107386417,2	K562	blood:
4	chr7:106685778..106688042-chr7:106804016..106805559,2	MCF-7	breast:
5	chr7:106683838..106685682-chr7:106808625..106810626,2	MCF-7	breast:
6	chr7:106415431..106417500-chr7:106684365..106686505,2	K562	blood:
7	chr7:106685221..106688860-chr7:106786297..106789878,4	K562	blood:
8	chr7:106682031..106689663-chr7:106807150..106811711,11	K562	blood:

Variant related genes	Relation type
PRKAR2B	TF binding region
PRKAR2B	CpG island
ENSG00000105879	chromatin interactions
ENSG00000228742	chromatin interactions
ENSG00000105856	chromatin interactions
ENSG00000241764	chromatin interactions

Extended variants
information (count: 64 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:64 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555721277	chr7:106684374-106684375	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs568418911	chr7:106684433-106684434	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537182349	chr7:106684541-106684542	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs564160525	chr7:106684575-106684576	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538659211	chr7:106684580-106684581	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs78715818	chr7:106684638-106684639	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs558744692	chr7:106684670-106684671	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs374914458	chr7:106684676-106684677	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182422019	chr7:106684686-106684687	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534897362	chr7:106684791-106684792	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs145100659	chr7:106684792-106684793	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185417000	chr7:106684807-106684808	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs543024807	chr7:106684844-106684845	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs77144210	chr7:106684931-106684932	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369611224	chr7:106684941-106684942	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576491854	chr7:106684966-106684967	Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546024974	chr7:106685034-106685035	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs559514855	chr7:106685039-106685040	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528784999	chr7:106685058-106685059	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs542492248	chr7:106685080-106685081	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562208384	chr7:106685134-106685135	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530958092	chr7:106685138-106685139	Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs112888336	chr7:106685207-106685208	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs550655408	chr7:106685254-106685255	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs570967400	chr7:106685256-106685257	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs200458097	chr7:106685342-106685343	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs370488960	chr7:106685362-106685363	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs373599721	chr7:106685382-106685383	Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs75727925	chr7:106685427-106685428	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs75385144	chr7:106685448-106685449	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs368313660	chr7:106685627-106685628	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs115878034	chr7:106685640-106685641	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs568215467	chr7:106685657-106685658	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs199823941	chr7:106685677-106685678	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs539687816	chr7:106685705-106685706	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs138906142	chr7:106685756-106685757	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs576579672	chr7:106685762-106685763	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs545473131	chr7:106685773-106685774	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs149409663	chr7:106685805-106685806	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs28546089	chr7:106685809-106685810	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542030608	chr7:106685837-106685838	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs562409623	chr7:106685857-106685858	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs531071569	chr7:106685861-106685862	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs77341403	chr7:106685880-106685881	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs564451163	chr7:106685906-106685907	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs181695642	chr7:106685907-106685908	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs35301821	chr7:106685910-106685911	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs547130288	chr7:106685946-106685947	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs566942050	chr7:106685949-106685950	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs536462773	chr7:106685976-106685977	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106676400-106684400	Weak transcription	NHLF	lung
2	chr7:106677000-106684400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:106677000-106684600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:106679600-106684400	Weak transcription	Fetal Stomach	stomach
5	chr7:106680000-106684400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:106680200-106684400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:106680400-106684400	Weak transcription	HUVEC	blood vessel
8	chr7:106681400-106684400	Weak transcription	Right Atrium	heart
9	chr7:106681600-106684400	Weak transcription	Adipose Nuclei	Adipose
10	chr7:106681800-106684400	Weak transcription	Stomach Mucosa	stomach
11	chr7:106682200-106684400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:106682400-106684600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr7:106682600-106684400	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:106683200-106684600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:106684000-106684400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:106684000-106684400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:106684000-106684400	Enhancers	Brain Germinal Matrix	brain
18	chr7:106684000-106684400	Enhancers	Fetal Kidney	kidney
19	chr7:106684000-106684400	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:106684000-106684400	Enhancers	Fetal Lung	lung
21	chr7:106684000-106685000	Flanking Active TSS	K562	blood
22	chr7:106684200-106684400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:106684200-106684400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:106684200-106684400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr7:106684200-106684400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr7:106684200-106684400	Enhancers	Primary T cells from cord blood	blood
27	chr7:106684200-106684400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr7:106684200-106684400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr7:106684200-106684400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:106684200-106684400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr7:106684200-106684400	Enhancers	Brain Cingulate Gyrus	brain
32	chr7:106684200-106684400	Enhancers	Colon Smooth Muscle	Colon
33	chr7:106684200-106684400	Enhancers	Fetal Brain Female	brain
34	chr7:106684200-106684400	Enhancers	NH-A	brain
35	chr7:106684200-106684600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:106684200-106685000	Flanking Active TSS	Fetal Brain Male	brain
37	chr7:106684200-106686400	Active TSS	Stomach Smooth Muscle	stomach
38	chr7:106684400-106684600	Active TSS	H1 Cell Line	embryonic stem cell
39	chr7:106684400-106684600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:106684400-106684600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
41	chr7:106684400-106684600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr7:106684400-106684600	Enhancers	Primary B cells from cord blood	blood
43	chr7:106684400-106684600	Enhancers	Primary T cells fromperipheralblood	blood
44	chr7:106684400-106684600	Enhancers	Primary hematopoietic stem cells	blood
45	chr7:106684400-106684600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:106684400-106684600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr7:106684400-106684600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:106684400-106684600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr7:106684400-106684600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr7:106684400-106684600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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