Variant report

Variant	esv9986
Chromosome Location	chr7:101971933-102004121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:993)
CpG islands
(count:488)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	chr7:102004002-102004510	A549	lung:	n/a	n/a
7	ATF3	chr7:102003901-102004509	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	chr7:101983890-101984191	GM12878	blood:	n/a	n/a
12	BATF	chr7:101997012-101997266	GM12878	blood:	n/a	n/a
13	BATF	chr7:101997851-101998066	GM12878	blood:	n/a	n/a
14	BATF	chr7:101982483-101982724	GM12878	blood:	n/a	n/a
15	BATF	chr7:101995463-101995686	GM12878	blood:	n/a	n/a
16	BATF	chr7:101980953-101981449	GM12878	blood:	n/a	n/a
17	BATF	chr7:101977330-101977583	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:102003799-102003974	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:101983901-101984172	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:101982462-101982707	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:101999465-101999748	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:101982419-101982753	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:101983656-101983848	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:101997984-101998246	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:101987225-101987383	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101996913-101997326	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:101994622-101994770	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:101999319-101999808	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:101981081-101981468	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:101975677-101976058	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:101987793-101988042	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:101975878-101976049	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:101977204-101977363	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:101992379-101992526	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:101997514-101997663	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:101981186-101981393	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:101983613-101984160	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:101990402-101990553	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:102003720-102004191	GM12878	blood:	n/a	n/a
40	BCL3	chr7:102003976-102004358	A549	lung:	n/a	n/a
41	BCLAF1	chr7:102003953-102004478	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:102003908-102004427	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:101997473-101997748	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:102004011-102004495	K562	blood:	n/a	n/a
45	BHLHE40	chr7:102004102-102004486	HepG2	liver:	n/a	n/a
46	BHLHE40	chr7:102004109-102004495	GM12878	blood:	n/a	n/a
47	BRCA1	chr7:102004018-102004395	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr7:102003731-102004487	K562	blood:	n/a	n/a
49	CBX3	chr7:102003667-102004553	K562	blood:	n/a	n/a
50	CEBPB	chr7:102003851-102004458	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102004098-102004148	H1-hESC	embryonic stem cell:	embryo
2	chr7:102004098-102004148	HAEpiC	amniotic membrane:	n/a
3	chr7:101998514-101998564	HRCEpiC	kidney:	n/a
4	chr7:101986487-101986537	AG09319	gingival:	n/a
5	chr7:101991189-101991239	NB4	blood:	n/a
6	chr7:101986487-101986537	ovcar-3	ovarian:	n/a
7	chr7:101989013-101989063	HCT-116	colon:	n/a
8	chr7:101991189-101991239	HIPEpiC	eye:	n/a
9	chr7:102004098-102004148	GM06990	blood:	n/a
10	chr7:101991189-101991239	HRCEpiC	kidney:	n/a
11	chr7:101989034-101989084	Hela-S3	cervix:	n/a
12	chr7:101999041-101999091	HCM	heart:	n/a
13	chr7:101972144-101972194	NHDF-neo	bronchial:	n/a
14	chr7:102004098-102004148	ovcar-3	ovarian:	n/a
15	chr7:101986487-101986537	RPTEC	kidney:	n/a
16	chr7:101991189-101991239	LNCaP	prostate:	n/a
17	chr7:101989013-101989063	NT2-D1	testis:	n/a
18	chr7:101989013-101989063	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:101972144-101972194	NB4	blood:	n/a
20	chr7:101986487-101986537	HRPEpiC	eye:	n/a
21	chr7:102004098-102004148	NHBE	bronchial:	n/a
22	chr7:101999041-101999091	HIPEpiC	eye:	n/a
23	chr7:101989034-101989084	HCT-116	colon:	n/a
24	chr7:102004098-102004148	HEK293	kidney:	embryo
25	chr7:101986487-101986537	HL-60	blood:	n/a
26	chr7:102004098-102004148	HL-60	blood:	n/a
27	chr7:101998514-101998564	HEEpiC	esophagus:	n/a
28	chr7:102004098-102004148	Hela-S3	cervix:	n/a
29	chr7:101998514-101998564	NHDF-neo	bronchial:	n/a
30	chr7:101986487-101986537	PrEC	prostate:	n/a
31	chr7:101991189-101991239	HCM	heart:	n/a
32	chr7:101972144-101972194	IMR90	lung:	fetal
33	chr7:102004098-102004148	Hepatocyte	liver:	n/a
34	chr7:101998514-101998564	HepG2	liver:	n/a
35	chr7:101991189-101991239	NHDF-neo	bronchial:	n/a
36	chr7:102004098-102004148	SAEC	small airway:	n/a
37	chr7:101972144-101972194	HepG2	liver:	n/a
38	chr7:101986487-101986537	NB4	blood:	n/a
39	chr7:101989034-101989084	SK-N-SH_RA	brain:	n/a
40	chr7:101989013-101989063	AG04450	lung:	fetal
41	chr7:101989034-101989084	HNPCEpiC	eye:	n/a
42	chr7:101998514-101998564	H1-hESC	embryonic stem cell:	embryo
43	chr7:101999041-101999091	ECC-1	luminal epithelium:	n/a
44	chr7:102004098-102004148	HEEpiC	esophagus:	n/a
45	chr7:101989013-101989063	HEK293	kidney:	embryo
46	chr7:102004098-102004148	SK-N-MC	brain:	n/a
47	chr7:102004098-102004148	HCF	heart:	n/a
48	chr7:101998514-101998564	BE2_C	brain:	n/a
49	chr7:101991189-101991239	PFSK-1	brain:	n/a
50	chr7:101998514-101998564	MCF10A-Er-Src	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:101965469..101968383-chr7:101972225..101973731,2	K562	blood:
2	chr7:101927779..101934386-chr7:102001430..102005829,12	MCF-7	breast:
3	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
4	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
5	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
ENSG00000160999	chromatin interactions
ENSG00000170409	chromatin interactions
ENSG00000239969	chromatin interactions
ENSG00000128563	chromatin interactions

Extended variants
information (count: 933 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147240083	chr7:101971968-101971969	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs140751609	chr7:101971974-101971975	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs535881541	chr7:101971987-101971988	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs554805702	chr7:101972000-101972001	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs191643153	chr7:101972016-101972017	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs2260832	chr7:101972037-101972038	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs112798273	chr7:101972062-101972063	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2260834	chr7:101972072-101972073	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs578129329	chr7:101972090-101972091	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144636659	chr7:101972120-101972121	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs147523503	chr7:101972136-101972137	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs2694167	chr7:101972153-101972154	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184680383	chr7:101972169-101972170	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561215551	chr7:101972193-101972194	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs531896716	chr7:101972217-101972218	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543593335	chr7:101972226-101972227	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs116675495	chr7:101972285-101972286	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs189051170	chr7:101972294-101972295	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs537512013	chr7:101972297-101972298	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs565643894	chr7:101972300-101972301	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs372838093	chr7:101972309-101972310	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs568767266	chr7:101972384-101972385	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs529663872	chr7:101972425-101972426	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs77060284	chr7:101972433-101972434	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs568142148	chr7:101972512-101972513	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs569951791	chr7:101972526-101972527	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs537373040	chr7:101972527-101972528	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs56055067	chr7:101972554-101972555	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs558781279	chr7:101972569-101972570	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs570665353	chr7:101972586-101972587	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs2529104	chr7:101972595-101972596	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs117353075	chr7:101972634-101972635	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs572467087	chr7:101972696-101972697	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs139413397	chr7:101972733-101972734	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs150032899	chr7:101972734-101972735	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs576304787	chr7:101972742-101972743	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs543749260	chr7:101972776-101972777	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs145377401	chr7:101972777-101972778	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs577323678	chr7:101972778-101972779	Enhancers Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs541290296	chr7:101972816-101972817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559365642	chr7:101972840-101972841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182000186	chr7:101972872-101972873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548187535	chr7:101972879-101972880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563321240	chr7:101972880-101972881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185622295	chr7:101972881-101972882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552459335	chr7:101972926-101972927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571961572	chr7:101972928-101972929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540239049	chr7:101972967-101972968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71286260	chr7:101972980-101972981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200024052	chr7:101973012-101973013	Weak transcription Enhancers	n/a	n/a	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:156 , 50 per page) page: 1 2 3 4

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	chr7:101968000-101975400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:101969200-101972200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:101970000-101972000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:101971600-101972600	Enhancers	Primary B cells from cord blood	blood
7	chr7:101971600-101972800	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:101971800-101972200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:101971800-101972600	Flanking Active TSS	GM12878-XiMat	blood
10	chr7:101971800-101974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:101972200-101972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:101972200-101972400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:101972200-101972600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:101972200-101972600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:101972200-101972800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:101972200-101972800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:101972200-101973400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:101972400-101972600	Enhancers	Fetal Kidney	kidney
19	chr7:101972600-101973400	Enhancers	GM12878-XiMat	blood
20	chr7:101972600-101973600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr7:101972800-101973600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:101972800-101973800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:101972800-101980800	Weak transcription	Primary B cells from peripheral blood	blood
24	chr7:101973200-101973600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:101973400-101973600	Enhancers	Fetal Kidney	kidney
26	chr7:101973400-101974200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:101973400-101975200	Weak transcription	GM12878-XiMat	blood
28	chr7:101973600-101974200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr7:101973600-101974800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:101973800-101974000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:101973800-101974000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:101974200-101974800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:101974800-101975000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:101974800-101975000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:101975000-101976400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:101975200-101976200	Enhancers	GM12878-XiMat	blood
37	chr7:101975400-101977200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:101976200-101981000	Weak transcription	GM12878-XiMat	blood
39	chr7:101980800-101983800	Enhancers	Primary B cells from peripheral blood	blood
40	chr7:101981000-101981800	Enhancers	GM12878-XiMat	blood
41	chr7:101981400-101981800	Enhancers	Primary B cells from cord blood	blood
42	chr7:101981800-101986000	Weak transcription	GM12878-XiMat	blood
43	chr7:101987400-102003800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr7:101987600-101990600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:101987600-101990600	Weak transcription	Liver	Liver
46	chr7:101987600-101990600	Weak transcription	Lung	lung
47	chr7:101987600-101990600	Weak transcription	Ovary	ovary
48	chr7:102002800-102003000	Enhancers	Left Ventricle	heart
49	chr7:102003400-102003800	Enhancers	Dnd41	blood
50	chr7:102003400-102004000	Enhancers	Primary T helper cells fromperipheralblood	blood

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