Variant report

Variant	nsv966866
Chromosome Location	chr7:99778337-99792754
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	chr7:99789523-99789556	K562	blood:	n/a	n/a
2	ARID3A	chr7:99787661-99788019	K562	blood:	n/a	n/a
3	ATF1	chr7:99787776-99787991	K562	blood:	n/a	n/a
4	ATF3	chr7:99787600-99788077	K562	blood:	n/a	n/a
5	BATF	chr7:99791718-99791975	GM12878	blood:	n/a	n/a
6	BATF	chr7:99791772-99792003	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:99789604-99789847	GM12878	blood:	n/a	n/a
8	BRCA1	chr7:99786769-99786836	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:99787685-99788065	K562	blood:	n/a	n/a
10	CEBPB	chr7:99789405-99790280	IMR90	lung:	n/a	chr7:99790097-99790108
11	CEBPB	chr7:99787718-99788137	A549	lung:	n/a	n/a
12	CEBPB	chr7:99789936-99790145	HepG2	liver:	n/a	chr7:99790097-99790108
13	CEBPB	chr7:99787728-99788031	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:99789984-99790178	K562	blood:	n/a	chr7:99790097-99790108
15	CEBPB	chr7:99787597-99788134	K562	blood:	n/a	n/a
16	CEBPB	chr7:99790089-99790135	H1-hESC	embryonic stem cell:	n/a	chr7:99790097-99790108
17	CEBPB	chr7:99789953-99790151	A549	lung:	n/a	chr7:99790097-99790108
18	CEBPB	chr7:99787684-99788054	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:99789943-99790236	K562	blood:	n/a	chr7:99790097-99790108
20	CEBPB	chr7:99787742-99788023	A549	lung:	n/a	n/a
21	CTCF	chr7:99787720-99787870	GM12872	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
22	CTCF	chr7:99787760-99787910	HA-sp	spinal cord:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
23	CTCF	chr7:99786560-99786710	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr7:99787734-99787926	LNCaP	prostate:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
25	CTCF	chr7:99787720-99787870	GM12871	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
26	CTCF	chr7:99787780-99787930	HCT-116	colon:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
27	CTCF	chr7:99787740-99787890	AG04450	lung:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
28	CTCF	chr7:99785160-99785310	GM12869	blood:	n/a	n/a
29	CTCF	chr7:99786780-99786930	AoAF	blood vessel:	n/a	chr7:99786859-99786868
30	CTCF	chr7:99787736-99787919	LNCaP	prostate:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
31	CTCF	chr7:99786960-99787110	HCM	heart:	n/a	n/a
32	CTCF	chr7:99787779-99787913	Kidney_OC	kidney:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
33	CTCF	chr7:99786800-99786950	GM12878	blood:	n/a	chr7:99786859-99786868
34	CTCF	chr7:99787940-99788090	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr7:99787778-99787921	MCF-7	breast:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
36	CTCF	chr7:99786800-99786950	HEEpiC	esophagus:	n/a	chr7:99786859-99786868
37	CTCF	chr7:99787760-99787910	BJ	skin:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
38	CTCF	chr7:99787800-99787950	GM12864	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
39	CTCF	chr7:99787761-99787929	GM13977	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
40	CTCF	chr7:99787740-99787890	HCT-116	colon:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
41	CTCF	chr7:99787791-99787845	GM20000	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
42	CTCF	chr7:99787800-99787950	GM12878	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
43	CTCF	chr7:99786540-99786690	HPF	lung:	n/a	n/a
44	CTCF	chr7:99786840-99786990	GM12865	blood:	n/a	chr7:99786859-99786868
45	CTCF	chr7:99787340-99787490	GM12872	blood:	n/a	n/a
46	CTCF	chr7:99787700-99787850	RPTEC	kidney:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
47	CTCF	chr7:99786840-99786990	HPF	lung:	n/a	chr7:99786859-99786868
48	CTCF	chr7:99787300-99787450	HVMF	connective:	n/a	n/a
49	CTCF	chr7:99787760-99787910	HAc	cerebellar:	n/a	chr7:99787827-99787843 chr7:99787826-99787844
50	CTCF	chr7:99787800-99787950	GM12874	blood:	n/a	chr7:99787827-99787843 chr7:99787826-99787844

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99778414-99778464	ovcar-3	ovarian:	n/a
2	chr7:99778414-99778464	U87	brain:	n/a
3	chr7:99778414-99778464	HepG2	liver:	n/a
4	chr7:99778414-99778464	Jurkat	blood:	n/a
5	chr7:99778414-99778464	HRCEpiC	kidney:	n/a
6	chr7:99778414-99778464	HCF	heart:	n/a
7	chr7:99778414-99778464	BJ	skin:	n/a
8	chr7:99778414-99778464	HUVEC	blood vessel:	n/a
9	chr7:99778414-99778464	Hela-S3	cervix:	n/a
10	chr7:99778414-99778464	MCF-7	breast:	n/a
11	chr7:99778414-99778464	RPTEC	kidney:	n/a
12	chr7:99778414-99778464	PrEC	prostate:	n/a
13	chr7:99778414-99778464	Hepatocyte	liver:	n/a
14	chr7:99778414-99778464	HL-60	blood:	n/a
15	chr7:99778414-99778464	SAEC	small airway:	n/a
16	chr7:99778414-99778464	AG09309	skin:	n/a
17	chr7:99778414-99778464	SK-N-SH_RA	brain:	n/a
18	chr7:99778414-99778464	HCT-116	colon:	n/a
19	chr7:99778414-99778464	PANC-1	pancreas:	n/a
20	chr7:99778414-99778464	AG04450	lung:	fetal
21	chr7:99778414-99778464	HEK293	kidney:	embryo
22	chr7:99778414-99778464	HRPEpiC	eye:	n/a
23	chr7:99778414-99778464	NT2-D1	testis:	n/a
24	chr7:99778414-99778464	CMK	blood:	n/a
25	chr7:99778414-99778464	AoSMC	blood vessel:	n/a
26	chr7:99778414-99778464	GM12878	blood:	n/a
27	chr7:99778414-99778464	MCF10A-Er-Src	breast:	n/a
28	chr7:99778414-99778464	K562	blood:	n/a
29	chr7:99778414-99778464	AG10803	skin:	n/a
30	chr7:99778414-99778464	GM06990	blood:	n/a
31	chr7:99778414-99778464	Caco-2	colon:	n/a
32	chr7:99778414-99778464	AG09319	gingival:	n/a
33	chr7:99778414-99778464	ProgFib	skin:	n/a
34	chr7:99778414-99778464	SKMC	muscle:	n/a
35	chr7:99778414-99778464	IMR90	lung:	fetal
36	chr7:99778414-99778464	NHDF-neo	bronchial:	n/a
37	chr7:99778414-99778464	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:99778414-99778464	LNCaP	prostate:	n/a
39	chr7:99778414-99778464	AG04449	skin:	fetal
40	chr7:99778414-99778464	PFSK-1	brain:	n/a
41	chr7:99778414-99778464	T-47D	breast:	n/a
42	chr7:99778414-99778464	HNPCEpiC	eye:	n/a
43	chr7:99778414-99778464	BE2_C	brain:	n/a
44	chr7:99778414-99778464	SK-N-MC	brain:	n/a
45	chr7:99778414-99778464	HRE	kidney:	n/a
46	chr7:99778414-99778464	HEEpiC	esophagus:	n/a
47	chr7:99778414-99778464	SK-N-SH	brain:	n/a
48	chr7:99778414-99778464	GM12892	blood:	n/a
49	chr7:99778414-99778464	A549	lung:	n/a
50	chr7:99778414-99778464	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:99761601..99763212-chr7:99780948..99783504,2	K562	blood:
2	chr7:99775409..99777327-chr7:99786470..99788338,2	K562	blood:
3	chr7:99754637..99756174-chr7:99779153..99781591,2	MCF-7	breast:
4	chr7:99781434..99783294-chr7:100007370..100009844,2	K562	blood:
5	chr7:99751463..99761050-chr7:99772463..99778676,10	K562	blood:
6	chr7:99788520..99793018-chr7:99795326..99799356,4	K562	blood:
7	chr7:99780980..99783660-chr7:99788379..99790159,2	K562	blood:
8	chr7:99789510..99791213-chr7:99808117..99810695,2	K562	blood:
9	chr7:99791489..99794024-chr7:99807798..99809792,2	K562	blood:
10	chr7:99772958..99774501-chr7:99782024..99784023,2	MCF-7	breast:
11	chr7:99773665..99775916-chr7:99787263..99789556,2	MCF-7	breast:
12	chr7:99745116..99747066-chr7:99785481..99787854,2	K562	blood:
13	chr7:99684721..99686749-chr7:99787610..99789461,2	K562	blood:
14	chr7:99780980..99783660-chr7:99788379..99790159,2	K562	blood:
15	chr7:99790117..99792841-chr7:99796413..99798138,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf59-1	chr7:99778116-99778518	NONHSAT122344

Variant related genes	Relation type
GPC2	TF binding region
STAG3	TF binding region
GPC2	CpG island
STAG3	CpG island
ENSG00000066923	chromatin interactions
ENSG00000239521	chromatin interactions
ENSG00000168090	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000266154	chromatin interactions
ENSG00000188186	chromatin interactions
ENSG00000213420	chromatin interactions

Extended variants
information (count: 543 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568326235	chr7:99778364-99778365	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs145715859	chr7:99778379-99778380	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs141506148	chr7:99778382-99778383	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs181266208	chr7:99778425-99778426	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs147067366	chr7:99778430-99778431	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs529822159	chr7:99778431-99778432	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs199911321	chr7:99778451-99778452	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs542123227	chr7:99778463-99778464	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs563395295	chr7:99778489-99778490	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs374295489	chr7:99778503-99778504	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs570876798	chr7:99778504-99778505	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs537799044	chr7:99778507-99778508	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs112086838	chr7:99778508-99778509	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs398067112	chr7:99778519-99778520	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs397890770	chr7:99778520-99778521	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs372731932	chr7:99778525-99778526	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs185854174	chr7:99778538-99778539	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs555894506	chr7:99778541-99778542	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs190278133	chr7:99778571-99778572	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs528176648	chr7:99778588-99778589	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs182867100	chr7:99778590-99778591	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs568096221	chr7:99778611-99778612	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs376021211	chr7:99778644-99778645	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs568657412	chr7:99778649-99778650	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs117677319	chr7:99778663-99778664	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs147687297	chr7:99778664-99778665	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs574465226	chr7:99778668-99778669	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs142571315	chr7:99778692-99778693	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs60966179	chr7:99778697-99778698	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs557716492	chr7:99778733-99778734	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs10229068	chr7:99778755-99778756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs541605984	chr7:99778770-99778771	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs148388695	chr7:99778772-99778773	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373091714	chr7:99778793-99778794	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs376956582	chr7:99778800-99778801	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs553916993	chr7:99778807-99778808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187596731	chr7:99778855-99778856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556443087	chr7:99778880-99778881	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs541612004	chr7:99778900-99778901	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs563645373	chr7:99778925-99778926	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs575599839	chr7:99778931-99778932	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs545847863	chr7:99778943-99778944	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs3807471	chr7:99778945-99778946	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs528061543	chr7:99779013-99779014	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546686295	chr7:99779028-99779029	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561584229	chr7:99779074-99779075	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs191848723	chr7:99779124-99779125	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs550887375	chr7:99779166-99779167	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs3779046	chr7:99779243-99779244	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs373675367	chr7:99779249-99779250	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Gastric cancer	24379144	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
Prostate cancer	16461572	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
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99775000-99780600	Enhancers	Primary T cells from cord blood	blood
2	chr7:99775800-99779400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr7:99775800-99787600	Weak transcription	GM12878-XiMat	blood
4	chr7:99775800-99798000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr7:99776000-99780400	Enhancers	Fetal Thymus	thymus
6	chr7:99776400-99778600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr7:99777600-99778800	Enhancers	Thymus	Thymus
8	chr7:99777800-99778800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:99777800-99779400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr7:99777800-99779600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr7:99778000-99778600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:99778000-99778800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:99778000-99778800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr7:99778000-99778800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr7:99778000-99779000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:99778000-99779200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr7:99778000-99779400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:99778000-99779400	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr7:99778200-99778400	Flanking Active TSS	Dnd41	blood
20	chr7:99778200-99778400	Enhancers	K562	blood
21	chr7:99778200-99778600	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:99778200-99778800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:99778200-99779800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:99778400-99778600	Enhancers	Dnd41	blood
25	chr7:99778400-99778800	Weak transcription	K562	blood
26	chr7:99778400-99779400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:99778400-99779600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:99778600-99778800	Flanking Active TSS	Dnd41	blood
29	chr7:99778600-99797800	Weak transcription	Fetal Intestine Small	intestine
30	chr7:99778800-99779400	Enhancers	Dnd41	blood
31	chr7:99778800-99780600	Enhancers	K562	blood
32	chr7:99778800-99787400	Weak transcription	Thymus	Thymus
33	chr7:99779000-99779200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr7:99779000-99779200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr7:99779000-99780200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:99779000-99780400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:99779000-99787400	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:99779200-99779400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:99779200-99779600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:99779200-99779800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr7:99779200-99779800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:99779200-99779800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:99779200-99780400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:99779200-99787800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:99779400-99779800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr7:99779400-99780600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr7:99779600-99779800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr7:99779600-99780000	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:99779800-99781000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr7:99780000-99780200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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