Variant report

Variant	esv3378448
Chromosome Location	chr7:99295540-99331065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99317835-99318286	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99330673-99331018	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:99311722-99312000	K562	blood:	n/a	n/a
4	ARID3A	chr7:99320919-99321131	K562	blood:	n/a	n/a
5	ARID3A	chr7:99327072-99327923	HepG2	liver:	n/a	n/a
6	ATF1	chr7:99320902-99321097	K562	blood:	n/a	n/a
7	BACH1	chr7:99317237-99317310	K562	blood:	n/a	n/a
8	BHLHE40	chr7:99327117-99327287	HepG2	liver:	n/a	n/a
9	CBX3	chr7:99325244-99325556	K562	blood:	n/a	n/a
10	CBX3	chr7:99325258-99325541	K562	blood:	n/a	n/a
11	CEBPB	chr7:99327052-99327479	HepG2	liver:	n/a	chr7:99327229-99327240
12	CEBPB	chr7:99317742-99317762	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:99327087-99327386	IMR90	lung:	n/a	chr7:99327229-99327240
14	CEBPB	chr7:99327000-99327473	HepG2	liver:	n/a	chr7:99327229-99327240
15	CEBPB	chr7:99327047-99327463	HepG2	liver:	n/a	chr7:99327229-99327240
16	CEBPB	chr7:99317967-99318253	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:99327036-99327520	MCF-7	breast:	n/a	chr7:99327229-99327240
18	CEBPB	chr7:99320854-99321043	K562	blood:	n/a	n/a
19	CEBPB	chr7:99326303-99326684	MCF-7	breast:	n/a	n/a
20	CEBPB	chr7:99326951-99327509	MCF-7	breast:	n/a	chr7:99327229-99327240
21	CEBPB	chr7:99327063-99327426	K562	blood:	n/a	chr7:99327229-99327240
22	CEBPB	chr7:99317988-99318190	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:99327060-99327428	K562	blood:	n/a	chr7:99327229-99327240
24	CEBPB	chr7:99327057-99327414	A549	lung:	n/a	chr7:99327229-99327240
25	CEBPB	chr7:99327013-99327588	Hela-S3	cervix:	n/a	chr7:99327229-99327240
26	CEBPB	chr7:99326912-99327416	HCT-116	colon:	n/a	chr7:99327229-99327240
27	CEBPB	chr7:99311647-99311995	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:99327125-99327423	H1-hESC	embryonic stem cell:	n/a	chr7:99327229-99327240
29	CEBPB	chr7:99327129-99327327	HepG2	liver:	n/a	chr7:99327229-99327240
30	CEBPD	chr7:99327137-99327400	HepG2	liver:	n/a	n/a
31	CEBPD	chr7:99320807-99321289	K562	blood:	n/a	n/a
32	CEBPD	chr7:99320807-99321231	K562	blood:	n/a	n/a
33	CEBPD	chr7:99327099-99327433	HepG2	liver:	n/a	n/a
34	CHD2	chr7:99327095-99327396	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:99311659-99311790	K562	blood:	n/a	n/a
36	CTCF	chr7:99330100-99330250	GM12871	blood:	n/a	n/a
37	CTCF	chr7:99313496-99313508	GM13976	blood:	n/a	n/a
38	CTCF	chr7:99330860-99331010	GM06990	blood:	n/a	n/a
39	CTCF	chr7:99325940-99326090	GM12869	blood:	n/a	n/a
40	CTCF	chr7:99307977-99307985	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:99330965-99331637	A549	lung:	n/a	chr7:99331308-99331317
42	CTCF	chr7:99311560-99311710	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr7:99329760-99329910	K562	blood:	n/a	n/a
44	CTCF	chr7:99311634-99311835	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:99317369-99317476	GM13976	blood:	n/a	n/a
46	CTCF	chr7:99311664-99311782	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:99331000-99331150	RPTEC	kidney:	n/a	n/a
48	CUX1	chr7:99320776-99321118	K562	blood:	n/a	n/a
49	CUX1	chr7:99297216-99297315	K562	blood:	n/a	n/a
50	E2F4	chr7:99302958-99303015	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99330962-99331012	HepG2	liver:	n/a
2	chr7:99302981-99303031	SK-N-MC	brain:	n/a
3	chr7:99330962-99331012	BE2_C	brain:	n/a
4	chr7:99330962-99331012	NT2-D1	testis:	n/a
5	chr7:99302981-99303031	HCT-116	colon:	n/a
6	chr7:99330962-99331012	LNCaP	prostate:	n/a
7	chr7:99302981-99303031	ProgFib	skin:	n/a
8	chr7:99302981-99303031	CMK	blood:	n/a
9	chr7:99302981-99303031	MCF-7	breast:	n/a
10	chr7:99302981-99303031	HCM	heart:	n/a
11	chr7:99302981-99303031	PrEC	prostate:	n/a
12	chr7:99302981-99303031	GM19239	blood:	n/a
13	chr7:99302981-99303031	AG09319	gingival:	n/a
14	chr7:99330962-99331012	AG10803	skin:	n/a
15	chr7:99330962-99331012	HRE	kidney:	n/a
16	chr7:99330962-99331012	T-47D	breast:	n/a
17	chr7:99330962-99331012	AG09319	gingival:	n/a
18	chr7:99302981-99303031	HEEpiC	esophagus:	n/a
19	chr7:99330962-99331012	GM06990	blood:	n/a
20	chr7:99330962-99331012	SAEC	small airway:	n/a
21	chr7:99302981-99303031	HIPEpiC	eye:	n/a
22	chr7:99302981-99303031	PANC-1	pancreas:	n/a
23	chr7:99302981-99303031	NT2-D1	testis:	n/a
24	chr7:99302981-99303031	Caco-2	colon:	n/a
25	chr7:99302981-99303031	IMR90	lung:	fetal
26	chr7:99302981-99303031	HMEC	breast:	n/a
27	chr7:99302981-99303031	SK-N-SH_RA	brain:	n/a
28	chr7:99330962-99331012	NH-A	brain:	n/a
29	chr7:99302981-99303031	GM06990	blood:	n/a
30	chr7:99302981-99303031	HepG2	liver:	n/a
31	chr7:99330962-99331012	U87	brain:	n/a
32	chr7:99330962-99331012	SK-N-MC	brain:	n/a
33	chr7:99302981-99303031	HRE	kidney:	n/a
34	chr7:99302981-99303031	LNCaP	prostate:	n/a
35	chr7:99330962-99331012	HRCEpiC	kidney:	n/a
36	chr7:99330962-99331012	NHBE	bronchial:	n/a
37	chr7:99302981-99303031	GM12878	blood:	n/a
38	chr7:99302981-99303031	AG04450	lung:	fetal
39	chr7:99302981-99303031	H1-hESC	embryonic stem cell:	embryo
40	chr7:99302981-99303031	NHBE	bronchial:	n/a
41	chr7:99302981-99303031	HAEpiC	amniotic membrane:	n/a
42	chr7:99330962-99331012	AG04450	lung:	fetal
43	chr7:99302981-99303031	NHDF-neo	bronchial:	n/a
44	chr7:99330962-99331012	CMK	blood:	n/a
45	chr7:99330962-99331012	HCF	heart:	n/a
46	chr7:99302981-99303031	SAEC	small airway:	n/a
47	chr7:99302981-99303031	HNPCEpiC	eye:	n/a
48	chr7:99302981-99303031	MCF10A-Er-Src	breast:	n/a
49	chr7:99302981-99303031	AG10803	skin:	n/a
50	chr7:99330962-99331012	Hepatocyte	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99299012..99301663-chr7:99302830..99305299,2	K562	blood:
2	chr7:99307529..99309266-chr7:99310963..99313906,2	K562	blood:
3	chr7:99307529..99309266-chr7:99310963..99313906,2	K562	blood:
4	chr7:99327792..99330076-chr7:99335753..99337453,2	K562	blood:
5	chr7:99304648..99307501-chr7:99308738..99311452,2	K562	blood:
6	chr7:99275381..99276881-chr7:99296561..99298122,2	MCF-7	breast:
7	chr7:99214549..99216608-chr7:99325712..99327239,2	MCF-7	breast:
8	chr7:99301150..99304477-chr7:99306434..99308951,3	K562	blood:
9	chr7:99296360..99298503-chr7:99313450..99315683,2	MCF-7	breast:
10	chr7:99301150..99304477-chr7:99306434..99308951,3	K562	blood:
11	chr7:99327130..99328855-chr7:99331843..99334078,2	K562	blood:
12	chr7:99299012..99301663-chr7:99302830..99305299,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A7-1	chr7:99328196-99328775	NONHSAT122271

No data

Variant related genes	Relation type
CYP3A7	TF binding region
ENSG00000221487	TF binding region
CYP3A7	CpG island
ENSG00000221487	CpG island
ENSG00000221487	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000160870	chromatin interactions

Extended variants
information (count: 1366 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10255749	chr7:99295550-99295551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563597492	chr7:99295551-99295552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374567176	chr7:99295653-99295654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566379717	chr7:99295669-99295670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2740564	chr7:99295693-99295694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554925713	chr7:99295700-99295701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370508356	chr7:99295701-99295702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140640525	chr7:99295702-99295703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150129905	chr7:99295703-99295704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs67709642	chr7:99295704-99295705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10629992	chr7:99295705-99295706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570098038	chr7:99295720-99295721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537532311	chr7:99295732-99295733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559140539	chr7:99295756-99295757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144870284	chr7:99295838-99295839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142064877	chr7:99295864-99295865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553746795	chr7:99295869-99295870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1851427	chr7:99295873-99295874	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542591695	chr7:99295888-99295889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560930993	chr7:99295989-99295990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531255574	chr7:99296022-99296023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543069027	chr7:99296042-99296043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10256572	chr7:99296069-99296070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs532533713	chr7:99296078-99296079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75724473	chr7:99296154-99296155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566169896	chr7:99296155-99296156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184601305	chr7:99296157-99296158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1818797	chr7:99296195-99296196	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs547876194	chr7:99296257-99296258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138865297	chr7:99296258-99296259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76015996	chr7:99296273-99296274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537443545	chr7:99296297-99296298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187783144	chr7:99296348-99296349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533361507	chr7:99296362-99296363	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs1818796	chr7:99296384-99296385	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538425662	chr7:99296425-99296426	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192529984	chr7:99296534-99296535	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572189134	chr7:99296544-99296545	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183651527	chr7:99296553-99296554	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554572151	chr7:99296622-99296623	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs2687085	chr7:99296686-99296687	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368535767	chr7:99296699-99296700	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543029985	chr7:99296744-99296745	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564610722	chr7:99296779-99296780	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs148058741	chr7:99296805-99296806	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2948344	chr7:99297011-99297012	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs559887627	chr7:99297018-99297019	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2948343	chr7:99297019-99297020	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs371812245	chr7:99297034-99297035	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189626244	chr7:99297045-99297046	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Urothelial carcinoma	21177765	CNVD
Congenital diaphragmatic hernia	21525063	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99277000-99295800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:99291400-99297600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:99291400-99297600	Weak transcription	Esophagus	oesophagus
4	chr7:99291400-99298800	Weak transcription	Aorta	Aorta
5	chr7:99291400-99306600	Weak transcription	Left Ventricle	heart
6	chr7:99291600-99295600	Weak transcription	Pancreas	Pancrea
7	chr7:99292200-99296200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:99292200-99296200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:99292200-99297000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:99292400-99295800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:99292400-99295800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:99292400-99295800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:99292400-99295800	Weak transcription	Stomach Mucosa	stomach
14	chr7:99292400-99296000	Weak transcription	A549	lung
15	chr7:99292400-99296400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:99292400-99298600	Enhancers	HepG2	liver
17	chr7:99293200-99295600	Weak transcription	Fetal Intestine Large	intestine
18	chr7:99293600-99296000	Weak transcription	Fetal Intestine Small	intestine
19	chr7:99293600-99297000	Weak transcription	Gastric	stomach
20	chr7:99294200-99301600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:99294400-99301400	Weak transcription	Liver	Liver
22	chr7:99294600-99295800	Weak transcription	K562	blood
23	chr7:99295600-99296000	Enhancers	Pancreas	Pancrea
24	chr7:99295600-99297600	Enhancers	Fetal Intestine Large	intestine
25	chr7:99295800-99296400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:99295800-99296400	Enhancers	Stomach Mucosa	stomach
27	chr7:99295800-99296800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr7:99295800-99297400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:99295800-99297400	Enhancers	Duodenum Mucosa	Duodenum
30	chr7:99295800-99297400	Enhancers	NHEK	skin
31	chr7:99295800-99297800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr7:99295800-99298200	Enhancers	K562	blood
33	chr7:99296000-99296400	Enhancers	A549	lung
34	chr7:99296000-99297400	Weak transcription	Pancreas	Pancrea
35	chr7:99296000-99297800	Enhancers	Fetal Intestine Small	intestine
36	chr7:99296200-99296400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr7:99296200-99297400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr7:99296200-99297800	Enhancers	Hela-S3	cervix
39	chr7:99296400-99296600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:99296400-99296600	Flanking Active TSS	A549	lung
41	chr7:99296400-99296800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr7:99296400-99296800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:99296400-99296800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:99296400-99296800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:99296400-99296800	Weak transcription	Stomach Mucosa	stomach
46	chr7:99296400-99296800	Enhancers	HUVEC	blood vessel
47	chr7:99296400-99297400	Enhancers	HMEC	breast
48	chr7:99296400-99297800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:99296400-99297800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:99296600-99297000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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