Variant report

Variant	esv3352723
Chromosome Location	chr7:101969387-102005026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1233)
CpG islands
(count:671)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102004022-102004495	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102004087-102004234	K562	blood:	n/a	n/a
3	ATF1	chr7:102003979-102004409	K562	blood:	n/a	n/a
4	ATF2	chr7:102003966-102004343	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:102003964-102004508	GM12878	blood:	n/a	n/a
6	ATF3	chr7:102003901-102004509	A549	lung:	n/a	n/a
7	ATF3	chr7:102004002-102004510	A549	lung:	n/a	n/a
8	ATF3	chr7:102004112-102004430	K562	blood:	n/a	n/a
9	BACH1	chr7:102004065-102004493	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:101999193-101999814	GM12878	blood:	n/a	n/a
11	BATF	chr7:102004902-102005484	GM12878	blood:	n/a	n/a
12	BATF	chr7:101982483-101982724	GM12878	blood:	n/a	n/a
13	BATF	chr7:101977330-101977583	GM12878	blood:	n/a	n/a
14	BATF	chr7:101995463-101995686	GM12878	blood:	n/a	n/a
15	BATF	chr7:101997012-101997266	GM12878	blood:	n/a	n/a
16	BATF	chr7:101980953-101981449	GM12878	blood:	n/a	n/a
17	BATF	chr7:101997851-101998066	GM12878	blood:	n/a	n/a
18	BATF	chr7:101983890-101984191	GM12878	blood:	n/a	n/a
19	BATF	chr7:102004126-102004439	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:101994622-101994770	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:101981186-101981393	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:101987225-101987383	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:101999465-101999748	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:102003720-102004191	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:101990402-101990553	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101983901-101984172	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:102003799-102003974	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:101982419-101982753	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:101996913-101997326	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:101982462-101982707	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:101987793-101988042	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:101983613-101984160	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:101999319-101999808	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:101983656-101983848	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:101977204-101977363	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:101997514-101997663	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:101975677-101976058	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:101975878-101976049	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:101992379-101992526	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102004788-102005191	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:101997984-101998246	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:101981081-101981468	GM12878	blood:	n/a	n/a
43	BCL3	chr7:102003976-102004358	A549	lung:	n/a	n/a
44	BCLAF1	chr7:102003908-102004427	GM12878	blood:	n/a	n/a
45	BCLAF1	chr7:102003953-102004478	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:102004102-102004486	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:102004011-102004495	K562	blood:	n/a	n/a
48	BHLHE40	chr7:101997473-101997748	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:102004109-102004495	GM12878	blood:	n/a	n/a
50	BRCA1	chr7:102004018-102004395	Hela-S3	cervix:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102005014-102005064	HCM	heart:	n/a
2	chr7:101998514-101998564	NH-A	brain:	n/a
3	chr7:101999041-101999091	HCT-116	colon:	n/a
4	chr7:101986487-101986537	Hela-S3	cervix:	n/a
5	chr7:101991189-101991239	HCT-116	colon:	n/a
6	chr7:101989013-101989063	HNPCEpiC	eye:	n/a
7	chr7:101989013-101989063	HCPEpiC	choroid plexus:	n/a
8	chr7:102004298-102004348	SAEC	small airway:	n/a
9	chr7:101986487-101986537	HRCEpiC	kidney:	n/a
10	chr7:102004298-102004348	LNCaP	prostate:	n/a
11	chr7:101991189-101991239	BJ	skin:	n/a
12	chr7:101989034-101989084	AG04449	skin:	fetal
13	chr7:102004775-102004825	HNPCEpiC	eye:	n/a
14	chr7:102004298-102004348	ECC-1	luminal epithelium:	n/a
15	chr7:101989034-101989084	ovcar-3	ovarian:	n/a
16	chr7:101989034-101989084	ProgFib	skin:	n/a
17	chr7:101989013-101989063	HRPEpiC	eye:	n/a
18	chr7:101989013-101989063	GM12891	blood:	n/a
19	chr7:101972144-101972194	HL-60	blood:	n/a
20	chr7:101989013-101989063	K562	blood:	n/a
21	chr7:102004298-102004348	MCF10A-Er-Src	breast:	n/a
22	chr7:102004098-102004148	AG04450	lung:	fetal
23	chr7:102005014-102005064	NB4	blood:	n/a
24	chr7:101991189-101991239	GM12892	blood:	n/a
25	chr7:101989013-101989063	AG10803	skin:	n/a
26	chr7:101989013-101989063	AG09319	gingival:	n/a
27	chr7:101972144-101972194	BE2_C	brain:	n/a
28	chr7:101989013-101989063	GM12878	blood:	n/a
29	chr7:102005014-102005064	AG04449	skin:	fetal
30	chr7:102004098-102004148	U87	brain:	n/a
31	chr7:101972144-101972194	SK-N-SH_RA	brain:	n/a
32	chr7:101972144-101972194	MCF10A-Er-Src	breast:	n/a
33	chr7:102004775-102004825	MCF10A-Er-Src	breast:	n/a
34	chr7:101989013-101989063	BJ	skin:	n/a
35	chr7:101989034-101989084	PrEC	prostate:	n/a
36	chr7:101986487-101986537	HCT-116	colon:	n/a
37	chr7:102004775-102004825	Hepatocyte	liver:	n/a
38	chr7:101999041-101999091	Hela-S3	cervix:	n/a
39	chr7:102004775-102004825	ProgFib	skin:	n/a
40	chr7:101972144-101972194	SAEC	small airway:	n/a
41	chr7:102004775-102004825	HL-60	blood:	n/a
42	chr7:101999041-101999091	SKMC	muscle:	n/a
43	chr7:101998514-101998564	AoSMC	blood vessel:	n/a
44	chr7:102004098-102004148	AG09319	gingival:	n/a
45	chr7:101972144-101972194	SKMC	muscle:	n/a
46	chr7:101999041-101999091	ovcar-3	ovarian:	n/a
47	chr7:102004775-102004825	LNCaP	prostate:	n/a
48	chr7:102004775-102004825	HCM	heart:	n/a
49	chr7:101989034-101989084	NHDF-neo	bronchial:	n/a
50	chr7:101999041-101999091	MCF10A-Er-Src	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:101965469..101968383-chr7:101972225..101973731,2	K562	blood:
2	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
3	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
4	chr7:101928261..101931030-chr7:101966781..101969545,2	K562	blood:
5	chr17:41465686..41466379-chr7:102004292..102004823,2	NB4	blood:
6	chr7:101927779..101934386-chr7:102001430..102005829,12	MCF-7	breast:
7	chr7:101962260..101964912-chr7:101971375..101973484,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIP1-1	chr7:101995384-101995807	ENSG00000259313.1
2	lnc-PRKRIP1-1	chr7:101993676-101993848	ENSG00000259313.1

No data

Variant related genes	Relation type
ENSG00000228546	TF binding region
ENSG00000200552	TF binding region
ENSG00000239969	TF binding region
SPDYE6	TF binding region
PRKRIP1	TF binding region
ENSG00000170409	TF binding region
ENSG00000228546	CpG island
ENSG00000200552	CpG island
ENSG00000239969	CpG island
SPDYE6	CpG island
PRKRIP1	CpG island
ENSG00000170409	CpG island
ENSG00000239969	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000170409	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000160999	chromatin interactions

Extended variants
information (count: 1085 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1085 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540210772	chr7:101969418-101969419	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs202038182	chr7:101969432-101969433	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2734625	chr7:101969436-101969437	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113882516	chr7:101969437-101969438	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200240805	chr7:101969438-101969439	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544221545	chr7:101969509-101969510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189490928	chr7:101969527-101969528	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532917146	chr7:101969528-101969529	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551182968	chr7:101969575-101969576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2529102	chr7:101969587-101969588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs803109	chr7:101969591-101969592	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546670419	chr7:101969597-101969598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546950803	chr7:101969599-101969600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565176544	chr7:101969608-101969609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536134500	chr7:101969650-101969651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535365796	chr7:101969662-101969663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557644751	chr7:101969667-101969668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181890578	chr7:101969668-101969669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532734036	chr7:101969687-101969688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs803110	chr7:101969693-101969694	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs803111	chr7:101969732-101969733	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150844052	chr7:101969749-101969750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555334127	chr7:101969773-101969774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368676943	chr7:101969774-101969775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548229883	chr7:101969792-101969793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs803112	chr7:101969809-101969810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543809673	chr7:101969909-101969910	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs28495216	chr7:101969914-101969915	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs2906696	chr7:101969920-101969921	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs803113	chr7:101969927-101969928	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs533071768	chr7:101969943-101969944	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2906697	chr7:101969952-101969953	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs544787514	chr7:101969953-101969954	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs559943582	chr7:101969998-101969999	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs577012042	chr7:101970003-101970004	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs528583326	chr7:101970016-101970017	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs546816556	chr7:101970021-101970022	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568547643	chr7:101970044-101970045	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186264174	chr7:101970045-101970046	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs551015158	chr7:101970046-101970047	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs569558794	chr7:101970065-101970066	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs190688073	chr7:101970069-101970070	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs558384334	chr7:101970099-101970100	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs2906699	chr7:101970106-101970107	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs566996539	chr7:101970113-101970114	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs2960253	chr7:101970114-101970115	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376272523	chr7:101970154-101970155	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs555123209	chr7:101970193-101970194	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs577554271	chr7:101970210-101970211	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs573704603	chr7:101970233-101970234	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
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
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101944000-101975400	Weak transcription	Right Atrium	heart
2	chr7:101962000-101973200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:101962800-101970800	Weak transcription	GM12878-XiMat	blood
4	chr7:101962800-101971600	Weak transcription	Primary B cells from cord blood	blood
5	chr7:101963200-101971600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr7:101963800-101971600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:101968000-101975400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:101968400-101970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr7:101969200-101972200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:101970000-101972000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:101970800-101971800	Enhancers	GM12878-XiMat	blood
12	chr7:101971600-101971800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:101971600-101972600	Enhancers	Primary B cells from cord blood	blood
14	chr7:101971600-101972800	Enhancers	Primary B cells from peripheral blood	blood
15	chr7:101971800-101972200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:101971800-101972600	Flanking Active TSS	GM12878-XiMat	blood
17	chr7:101971800-101974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:101972200-101972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:101972200-101972400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:101972200-101972600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:101972200-101972600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:101972200-101972800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:101972200-101972800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:101972200-101973400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:101972400-101972600	Enhancers	Fetal Kidney	kidney
26	chr7:101972600-101973400	Enhancers	GM12878-XiMat	blood
27	chr7:101972600-101973600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:101972800-101973600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:101972800-101973800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr7:101972800-101980800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr7:101973200-101973600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:101973400-101973600	Enhancers	Fetal Kidney	kidney
33	chr7:101973400-101974200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:101973400-101975200	Weak transcription	GM12878-XiMat	blood
35	chr7:101973600-101974200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:101973600-101974800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:101973800-101974000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:101973800-101974000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:101974200-101974800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:101974800-101975000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:101974800-101975000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:101975000-101976400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:101975200-101976200	Enhancers	GM12878-XiMat	blood
44	chr7:101975400-101977200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:101976200-101981000	Weak transcription	GM12878-XiMat	blood
46	chr7:101980800-101983800	Enhancers	Primary B cells from peripheral blood	blood
47	chr7:101981000-101981800	Enhancers	GM12878-XiMat	blood
48	chr7:101981400-101981800	Enhancers	Primary B cells from cord blood	blood
49	chr7:101981800-101986000	Weak transcription	GM12878-XiMat	blood
50	chr7:101987400-102003800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links