Variant report

Variant	esv3385336
Chromosome Location	chr7:100134766-100138414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:489)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:100135811-100135972	K562	blood:	n/a	n/a
2	ARID3A	chr7:100138141-100138175	K562	blood:	n/a	n/a
3	ARID3A	chr7:100136214-100136769	K562	blood:	n/a	n/a
4	ARID3A	chr7:100136328-100136969	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:100137501-100138363	HepG2	liver:	n/a	n/a
6	ATF1	chr7:100136099-100136851	K562	blood:	n/a	n/a
7	ATF2	chr7:100136137-100136548	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:100136155-100136633	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:100136249-100136568	GM12878	blood:	n/a	n/a
10	ATF2	chr7:100136614-100136985	GM12878	blood:	n/a	n/a
11	BACH1	chr7:100137414-100137664	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:100136462-100136570	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:100137042-100137102	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr7:100136011-100136613	A549	lung:	n/a	n/a
15	BHLHE40	chr7:100136100-100137135	K562	blood:	n/a	n/a
16	BHLHE40	chr7:100136306-100136999	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:100137869-100138042	HepG2	liver:	n/a	n/a
18	BHLHE40	chr7:100136275-100137018	A549	lung:	n/a	n/a
19	BHLHE40	chr7:100136228-100137096	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:100136188-100136913	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:100136422-100136622	GM12878	blood:	n/a	n/a
22	BRCA1	chr7:100136317-100136584	HepG2	liver:	n/a	n/a
23	CBX3	chr7:100135973-100136613	K562	blood:	n/a	n/a
24	CBX3	chr7:100135905-100137096	K562	blood:	n/a	n/a
25	CCNT2	chr7:100136417-100137180	K562	blood:	n/a	chr7:100136626-100136635
26	CEBPB	chr7:100136314-100136536	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:100137722-100138042	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:100137708-100138083	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:100136294-100136611	K562	blood:	n/a	chr7:100136538-100136546
30	CEBPB	chr7:100136097-100136821	K562	blood:	n/a	chr7:100136793-100136801 chr7:100136538-100136546
31	CEBPB	chr7:100136260-100136933	Hela-S3	cervix:	n/a	chr7:100136793-100136801 chr7:100136538-100136546
32	CEBPB	chr7:100137761-100138056	A549	lung:	n/a	n/a
33	CEBPB	chr7:100137708-100138025	K562	blood:	n/a	n/a
34	CEBPB	chr7:100137702-100138093	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:100137700-100138073	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:100137646-100138149	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:100137674-100138114	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:100137760-100138039	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:100135989-100136440	GM12878	blood:	n/a	n/a
40	CEBPD	chr7:100136788-100136982	HepG2	liver:	n/a	n/a
41	CEBPD	chr7:100137649-100137997	HepG2	liver:	n/a	n/a
42	CEBPD	chr7:100136685-100137069	HepG2	liver:	n/a	n/a
43	CHD1	chr7:100136872-100137031	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr7:100136895-100137064	GM12878	blood:	n/a	n/a
45	CHD2	chr7:100136260-100136971	K562	blood:	n/a	n/a
46	CHD2	chr7:100136271-100136979	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr7:100136247-100136994	GM12878	blood:	n/a	n/a
48	CHD2	chr7:100136346-100136720	HepG2	liver:	n/a	n/a
49	CHD2	chr7:100136305-100136990	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr7:100136141-100137126	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100136168-100136218	K562	blood:	n/a
2	chr7:100136168-100136218	K562	blood:	n/a
3	chr7:100136168-100136218	RPTEC	kidney:	n/a
4	chr7:100136013-100136063	HUVEC	blood vessel:	n/a
5	chr7:100136168-100136218	GM12892	blood:	n/a
6	chr7:100136168-100136218	NT2-D1	testis:	n/a
7	chr7:100136517-100136567	SK-N-SH	brain:	n/a
8	chr7:100136710-100136760	HNPCEpiC	eye:	n/a
9	chr7:100136168-100136218	GM12878	blood:	n/a
10	chr7:100136517-100136567	HUVEC	blood vessel:	n/a
11	chr7:100136710-100136760	GM12891	blood:	n/a
12	chr7:100136168-100136218	MCF10A-Er-Src	breast:	n/a
13	chr7:100137102-100137152	SK-N-SH_RA	brain:	n/a
14	chr7:100136910-100136960	GM06990	blood:	n/a
15	chr7:100136710-100136760	CMK	blood:	n/a
16	chr7:100136710-100136760	HepG2	liver:	n/a
17	chr7:100136710-100136760	SK-N-SH_RA	brain:	n/a
18	chr7:100136168-100136218	AG04450	lung:	fetal
19	chr7:100136710-100136760	NH-A	brain:	n/a
20	chr7:100136742-100136792	MCF10A-Er-Src	breast:	n/a
21	chr7:100136168-100136218	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:100136742-100136792	AoSMC	blood vessel:	n/a
23	chr7:100136168-100136218	PANC-1	pancreas:	n/a
24	chr7:100136517-100136567	HCF	heart:	n/a
25	chr7:100136910-100136960	A549	lung:	n/a
26	chr7:100136168-100136218	Caco-2	colon:	n/a
27	chr7:100136517-100136567	PrEC	prostate:	n/a
28	chr7:100137102-100137152	AoSMC	blood vessel:	n/a
29	chr7:100136517-100136567	ECC-1	luminal epithelium:	n/a
30	chr7:100136710-100136760	HMEC	breast:	n/a
31	chr7:100136710-100136760	PrEC	prostate:	n/a
32	chr7:100136013-100136063	MCF-7	breast:	n/a
33	chr7:100136742-100136792	NH-A	brain:	n/a
34	chr7:100136710-100136760	IMR90	lung:	fetal
35	chr7:100136710-100136760	Hela-S3	cervix:	n/a
36	chr7:100136013-100136063	MCF10A-Er-Src	breast:	n/a
37	chr7:100136013-100136063	A549	lung:	n/a
38	chr7:100137102-100137152	HIPEpiC	eye:	n/a
39	chr7:100136710-100136760	NHDF-neo	bronchial:	n/a
40	chr7:100136768-100136818	SK-N-SH_RA	brain:	n/a
41	chr7:100136710-100136760	BE2_C	brain:	n/a
42	chr7:100136013-100136063	NHBE	bronchial:	n/a
43	chr7:100136768-100136818	HMEC	breast:	n/a
44	chr7:100136742-100136792	CMK	blood:	n/a
45	chr7:100136013-100136063	NB4	blood:	n/a
46	chr7:100136768-100136818	BJ	skin:	n/a
47	chr7:100136013-100136063	HRPEpiC	eye:	n/a
48	chr7:100136910-100136960	CMK	blood:	n/a
49	chr7:100136168-100136218	HL-60	blood:	n/a
50	chr7:100136710-100136760	HEEpiC	esophagus:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100135274..100138223-chr7:100165794..100167927,2	MCF-7	breast:
2	chr7:100080596..100081585-chr7:100136654..100137320,2	K562	blood:
3	chr7:100136348..100138859-chr7:100182557..100185063,3	MCF-7	breast:
4	chr7:100127022..100128538-chr7:100137824..100140499,2	MCF-7	breast:
5	chr7:26240257..26240815-chr7:100136639..100137141,2	Hela-S3	cervix:
6	chr7:100081136..100082649-chr7:100135146..100137776,2	K562	blood:
7	chr7:100081083..100081652-chr7:100135891..100136813,2	NB4	blood:
8	chr7:100135877..100137947-chr7:100173185..100175230,2	K562	blood:
9	chr7:100134485..100137368-chr7:100183364..100186308,2	K562	blood:
10	chr7:100136576..100139151-chr7:100200299..100204148,3	K562	blood:
11	chr7:100025714..100030196-chr7:100134897..100138793,5	K562	blood:
12	chr7:100073864..100076959-chr7:100134677..100138430,3	K562	blood:
13	chr7:100135868..100137929-chr7:100182760..100184864,2	K562	blood:
14	chr7:100081136..100082722-chr7:100136276..100137942,2	K562	blood:
15	chr7:100080256..100081975-chr7:100135714..100137947,2	MCF-7	breast:
16	chr7:100074273..100077650-chr7:100135969..100140252,4	MCF-7	breast:

No data

Variant related genes	Relation type
AGFG2	TF binding region
AGFG2	CpG island
ENSG00000106333	chromatin interactions
ENSG00000166925	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000166924	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000184414	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000242101	chromatin interactions
ENSG00000224729	chromatin interactions
ENSG00000266372	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000122565	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554121022	chr7:100134766-100134767	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs540373920	chr7:100134769-100134770	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs561656944	chr7:100134779-100134780	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs572375960	chr7:100134785-100134786	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs528888890	chr7:100134787-100134788	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs544841725	chr7:100134790-100134791	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs563058357	chr7:100134798-100134799	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs533718378	chr7:100134799-100134800	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs551539244	chr7:100134802-100134803	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs374645644	chr7:100134809-100134810	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs368962483	chr7:100134819-100134820	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs386716125	chr7:100134831-100134832	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs373402893	chr7:100134854-100134855	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs377570393	chr7:100134863-100134864	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs536907277	chr7:100134865-100134866	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs567275540	chr7:100134876-100134877	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs537875327	chr7:100134877-100134878	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs370740215	chr7:100134890-100134891	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs569040534	chr7:100134908-100134909	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs539747320	chr7:100134919-100134920	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs7805498	chr7:100134920-100134921	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
22	rs187869586	chr7:100134952-100134953	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs533829493	chr7:100134964-100134965	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs555502322	chr7:100135004-100135005	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs74698925	chr7:100135031-100135032	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs573550769	chr7:100135033-100135034	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs543851455	chr7:100135035-100135036	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs150404034	chr7:100135061-100135062	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs578186405	chr7:100135063-100135064	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs545335231	chr7:100135077-100135078	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs35052680	chr7:100135105-100135106	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs560274549	chr7:100135118-100135119	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs191229149	chr7:100135166-100135167	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs199720946	chr7:100135178-100135179	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs114795085	chr7:100135180-100135181	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs115704946	chr7:100135205-100135206	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs543536245	chr7:100135226-100135227	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs183772682	chr7:100135289-100135290	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs549884780	chr7:100135290-100135291	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs187013350	chr7:100135293-100135294	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs539733834	chr7:100135338-100135339	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs551708620	chr7:100135392-100135393	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs35817935	chr7:100135404-100135405	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs565129544	chr7:100135427-100135428	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs113379331	chr7:100135433-100135434	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs566620232	chr7:100135470-100135471	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs561785437	chr7:100135531-100135532	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs533996906	chr7:100135548-100135549	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs555636941	chr7:100135603-100135604	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs573636578	chr7:100135641-100135642	Weak transcription Enhancers	Chromatin interactive region	8 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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100091800-100136200	Weak transcription	Right Atrium	heart
2	chr7:100125800-100136000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:100129800-100136000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:100131200-100136000	Weak transcription	Colonic Mucosa	Colon
5	chr7:100131200-100136000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:100131200-100136000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:100131400-100136000	Weak transcription	Stomach Mucosa	stomach
8	chr7:100131800-100136000	Weak transcription	Fetal Heart	heart
9	chr7:100132200-100136000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:100132800-100136000	Weak transcription	Right Ventricle	heart
11	chr7:100133000-100136000	Weak transcription	Liver	Liver
12	chr7:100133000-100136000	Weak transcription	Fetal Intestine Large	intestine
13	chr7:100133000-100136000	Weak transcription	Fetal Intestine Small	intestine
14	chr7:100133600-100135800	Weak transcription	HepG2	liver
15	chr7:100133800-100135800	Weak transcription	K562	blood
16	chr7:100135600-100135800	Enhancers	Dnd41	blood
17	chr7:100135800-100136000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:100135800-100136000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:100135800-100136000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:100135800-100136000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:100135800-100136000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:100135800-100136000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:100135800-100136000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:100135800-100136000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:100135800-100136000	Enhancers	Primary B cells from cord blood	blood
26	chr7:100135800-100136000	Enhancers	Primary T cells from cord blood	blood
27	chr7:100135800-100136000	Enhancers	Primary hematopoietic stem cells	blood
28	chr7:100135800-100136000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:100135800-100136000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:100135800-100136000	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr7:100135800-100136000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr7:100135800-100136000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:100135800-100136000	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr7:100135800-100136000	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr7:100135800-100136000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr7:100135800-100136000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:100135800-100136000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr7:100135800-100136000	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr7:100135800-100136000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:100135800-100136000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:100135800-100136000	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:100135800-100136000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:100135800-100136000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:100135800-100136000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:100135800-100136000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:100135800-100136000	Enhancers	Adipose Nuclei	Adipose
47	chr7:100135800-100136000	Enhancers	Brain Angular Gyrus	brain
48	chr7:100135800-100136000	Enhancers	Brain Anterior Caudate	brain
49	chr7:100135800-100136000	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:100135800-100136000	Enhancers	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links