Variant report

Variant	nsv437032
Chromosome Location	chr7:137753091-137773291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137771010-137771910	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:137771365-137771615	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:137758776-137759144	MCF-7	breast:	n/a	n/a
4	CEBPB	chr7:137762614-137762981	HepG2	liver:	n/a	chr7:137762763-137762774
5	CEBPB	chr7:137762615-137762916	HepG2	liver:	n/a	chr7:137762763-137762774
6	CEBPB	chr7:137771338-137771712	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:137771370-137771691	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:137765131-137765198	HepG2	liver:	n/a	chr7:137765148-137765161 chr7:137765148-137765161 chr7:137765148-137765159 chr7:137765149-137765160 chr7:137765148-137765159
9	CEBPB	chr7:137762629-137762910	A549	lung:	n/a	chr7:137762763-137762774
10	CEBPB	chr7:137762632-137762892	K562	blood:	n/a	chr7:137762763-137762774
11	CEBPB	chr7:137762620-137762839	HepG2	liver:	n/a	chr7:137762763-137762774
12	CEBPB	chr7:137762642-137762897	IMR90	lung:	n/a	chr7:137762763-137762774
13	CEBPB	chr7:137762610-137763408	Hela-S3	cervix:	n/a	chr7:137762763-137762774
14	CEBPB	chr7:137758745-137758864	A549	lung:	n/a	n/a
15	CEBPB	chr7:137771370-137771633	HepG2	liver:	n/a	n/a
16	CEBPD	chr7:137771361-137771599	HepG2	liver:	n/a	n/a
17	CHD2	chr7:137762679-137762879	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr7:137755065-137755066	K562	blood:	n/a	n/a
19	CTCF	chr7:137771902-137772090	HepG2	liver:	n/a	n/a
20	CTCF	chr7:137771900-137772050	MCF-7	breast:	n/a	n/a
21	CTCF	chr7:137765880-137766030	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:137771929-137772027	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:137771949-137772030	HepG2	liver:	n/a	n/a
24	EBF1	chr7:137768677-137768877	GM12878	blood:	n/a	chr7:137768754-137768763 chr7:137768753-137768764
25	EP300	chr7:137758756-137759415	MCF-7	breast:	n/a	n/a
26	EP300	chr7:137762615-137762897	Hela-S3	cervix:	n/a	chr7:137762617-137762630
27	EP300	chr7:137758684-137759134	HepG2	liver:	n/a	n/a
28	EP300	chr7:137771223-137772038	HepG2	liver:	n/a	n/a
29	EP300	chr7:137762482-137762895	HepG2	liver:	n/a	chr7:137762617-137762630
30	EP300	chr7:137771343-137771630	HepG2	liver:	n/a	n/a
31	EP300	chr7:137762497-137762899	HepG2	liver:	n/a	chr7:137762617-137762630
32	EP300	chr7:137760857-137761374	HepG2	liver:	n/a	n/a
33	ESR1	chr7:137759171-137759486	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr7:137759174-137759427	ECC-1	luminal epithelium:	n/a	n/a
35	FOS	chr7:137762611-137763311	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr7:137758933-137759202	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr7:137759051-137759264	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr7:137762611-137763369	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr7:137762634-137762925	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr7:137762622-137762920	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr7:137759128-137759310	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA1	chr7:137758726-137759057	T-47D	breast:	n/a	n/a
43	FOXA1	chr7:137771283-137771616	HepG2	liver:	n/a	n/a
44	FOXA1	chr7:137758666-137759208	HepG2	liver:	n/a	chr7:137759052-137759067
45	FOXA1	chr7:137771208-137771615	HepG2	liver:	n/a	n/a
46	FOXA1	chr7:137758780-137759102	T-47D	breast:	n/a	chr7:137759052-137759067
47	FOXA1	chr7:137771217-137771738	HepG2	liver:	n/a	n/a
48	FOXA1	chr7:137762472-137762904	HepG2	liver:	n/a	n/a
49	FOXA1	chr7:137771248-137771602	HepG2	liver:	n/a	n/a
50	FOXA1	chr7:137762448-137762921	HepG2	liver:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137757578-137757628	BE2_C	brain:	n/a
2	chr7:137760222-137760272	IMR90	lung:	fetal
3	chr7:137760331-137760381	GM06990	blood:	n/a
4	chr7:137760128-137760178	HAEpiC	amniotic membrane:	n/a
5	chr7:137761289-137761339	HRPEpiC	eye:	n/a
6	chr7:137757578-137757628	HRCEpiC	kidney:	n/a
7	chr7:137760222-137760272	BJ	skin:	n/a
8	chr7:137760128-137760178	GM12892	blood:	n/a
9	chr7:137766315-137766365	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:137761047-137761097	HRPEpiC	eye:	n/a
11	chr7:137757578-137757628	GM12892	blood:	n/a
12	chr7:137760222-137760272	T-47D	breast:	n/a
13	chr7:137760222-137760272	SAEC	small airway:	n/a
14	chr7:137760222-137760272	HRPEpiC	eye:	n/a
15	chr7:137761047-137761097	Jurkat	blood:	n/a
16	chr7:137757578-137757628	MCF-7	breast:	n/a
17	chr7:137760222-137760272	HNPCEpiC	eye:	n/a
18	chr7:137760128-137760178	ovcar-3	ovarian:	n/a
19	chr7:137761047-137761097	HCPEpiC	choroid plexus:	n/a
20	chr7:137760128-137760178	AG10803	skin:	n/a
21	chr7:137760222-137760272	HCPEpiC	choroid plexus:	n/a
22	chr7:137766315-137766365	K562	blood:	n/a
23	chr7:137760128-137760178	CMK	blood:	n/a
24	chr7:137766315-137766365	MCF-7	breast:	n/a
25	chr7:137757578-137757628	ProgFib	skin:	n/a
26	chr7:137761289-137761339	GM06990	blood:	n/a
27	chr7:137760331-137760381	HRE	kidney:	n/a
28	chr7:137757578-137757628	HRPEpiC	eye:	n/a
29	chr7:137760222-137760272	AG09319	gingival:	n/a
30	chr7:137761047-137761097	Hela-S3	cervix:	n/a
31	chr7:137761289-137761339	SK-N-SH	brain:	n/a
32	chr7:137760128-137760178	GM19239	blood:	n/a
33	chr7:137760128-137760178	AoSMC	blood vessel:	n/a
34	chr7:137761289-137761339	GM12878	blood:	n/a
35	chr7:137760222-137760272	HCT-116	colon:	n/a
36	chr7:137761047-137761097	AG04450	lung:	fetal
37	chr7:137757578-137757628	HCF	heart:	n/a
38	chr7:137757578-137757628	U87	brain:	n/a
39	chr7:137760128-137760178	H1-hESC	embryonic stem cell:	embryo
40	chr7:137761047-137761097	PrEC	prostate:	n/a
41	chr7:137760128-137760178	MCF-7	breast:	n/a
42	chr7:137761289-137761339	NHDF-neo	bronchial:	n/a
43	chr7:137757578-137757628	HCT-116	colon:	n/a
44	chr7:137761047-137761097	LNCaP	prostate:	n/a
45	chr7:137757578-137757628	ECC-1	luminal epithelium:	n/a
46	chr7:137761047-137761097	HRE	kidney:	n/a
47	chr7:137766315-137766365	Caco-2	colon:	n/a
48	chr7:137761047-137761097	HUVEC	blood vessel:	n/a
49	chr7:137760331-137760381	HepG2	liver:	n/a
50	chr7:137766315-137766365	Hela-S3	cervix:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137758486..137761270-chr7:137763871..137767061,3	K562	blood:
2	chr7:137750905..137753391-chr7:137753701..137756369,2	MCF-7	breast:
3	chr7:137769402..137771015-chr7:137771922..137774982,3	MCF-7	breast:
4	chr7:137746837..137750836-chr7:137772601..137775949,4	MCF-7	breast:
5	chr7:137761079..137762998-chr7:137763211..137766028,2	MCF-7	breast:
6	chr7:137747667..137753748-chr7:137756655..137760355,9	MCF-7	breast:
7	chr7:137686258..137688306-chr7:137772925..137775024,2	MCF-7	breast:
8	chr7:137769402..137771015-chr7:137771922..137774982,3	MCF-7	breast:
9	chr7:137759066..137761270-chr7:137763871..137766101,2	K562	blood:
10	chr7:137745328..137748047-chr7:137765457..137767555,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221558	TF binding region
AKR1D1	TF binding region
RN7SKP223	TF binding region
ENSG00000221558	CpG island
AKR1D1	CpG island
RN7SKP223	CpG island
ENSG00000221558	chromatin interactions
ENSG00000182158	chromatin interactions
ENSG00000122787	chromatin interactions

Extended variants
information (count: 726 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1025967	chr7:137753091-137753092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556605016	chr7:137753096-137753097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs575859952	chr7:137753102-137753103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs144499830	chr7:137753107-137753108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs73449463	chr7:137753150-137753151	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs78112930	chr7:137753186-137753187	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs181098924	chr7:137753193-137753194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs75756344	chr7:137753225-137753226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs546687243	chr7:137753338-137753339	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs370580024	chr7:137753366-137753367	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs199679848	chr7:137753383-137753384	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs10265064	chr7:137753520-137753521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs10954601	chr7:137753539-137753540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs186029632	chr7:137753547-137753548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs148426434	chr7:137753610-137753611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558169565	chr7:137753617-137753618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73732233	chr7:137753619-137753620	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs1487999	chr7:137753620-137753621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551964416	chr7:137753664-137753665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7812287	chr7:137753675-137753676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs189306230	chr7:137753685-137753686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548061108	chr7:137753728-137753729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1488000	chr7:137753778-137753779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567586296	chr7:137753814-137753815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536627154	chr7:137753818-137753819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116031215	chr7:137754025-137754026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374422956	chr7:137754071-137754072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182141149	chr7:137754072-137754073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558281242	chr7:137754083-137754084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145932558	chr7:137754092-137754093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187376625	chr7:137754097-137754098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4732285	chr7:137754127-137754128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534648006	chr7:137754140-137754141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149537762	chr7:137754165-137754166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114870533	chr7:137754174-137754175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574373519	chr7:137754246-137754247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139776102	chr7:137754315-137754316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573826260	chr7:137754325-137754326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144521983	chr7:137754330-137754331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576966708	chr7:137754373-137754374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190804439	chr7:137754415-137754416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542463198	chr7:137754418-137754419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs115539959	chr7:137754433-137754434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs116358990	chr7:137754473-137754474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146628491	chr7:137754481-137754482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373482572	chr7:137754505-137754506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs553016749	chr7:137754515-137754516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141047326	chr7:137754553-137754554	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182951981	chr7:137754597-137754598	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368120181	chr7:137754598-137754599	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137750000-137756200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr7:137750000-137756400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:137750200-137756000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:137751000-137753600	Flanking Active TSS	HepG2	liver
5	chr7:137751200-137754000	Enhancers	Liver	Liver
6	chr7:137752600-137754600	Enhancers	Fetal Intestine Large	intestine
7	chr7:137753600-137754800	Enhancers	HepG2	liver
8	chr7:137754000-137758800	Weak transcription	Liver	Liver
9	chr7:137754800-137756600	Genic enhancers	HepG2	liver
10	chr7:137755800-137758000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:137756000-137758000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:137756000-137758200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:137756200-137756400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:137756200-137756800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:137756200-137758000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:137756400-137757400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:137756400-137758000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:137756600-137757800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr7:137756600-137758600	Weak transcription	HepG2	liver
20	chr7:137756800-137757800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:137757000-137757200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:137757400-137757600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr7:137757600-137759600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr7:137757800-137761200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr7:137758000-137760200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr7:137758600-137759800	Enhancers	HMEC	breast
27	chr7:137758600-137761200	ZNF genes & repeats	HepG2	liver
28	chr7:137758800-137759200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:137758800-137759200	Flanking Active TSS	Liver	Liver
30	chr7:137758800-137759400	Enhancers	Hela-S3	cervix
31	chr7:137759000-137760600	Enhancers	Primary B cells from peripheral blood	blood
32	chr7:137759200-137759600	Enhancers	NHEK	skin
33	chr7:137759200-137760600	ZNF genes & repeats	GM12878-XiMat	blood
34	chr7:137759200-137760800	Enhancers	Liver	Liver
35	chr7:137759200-137761400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:137759200-137762400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:137759400-137760600	Enhancers	Primary B cells from cord blood	blood
38	chr7:137759400-137762400	Weak transcription	Hela-S3	cervix
39	chr7:137760000-137760800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr7:137760200-137761200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr7:137760800-137761200	Flanking Active TSS	Liver	Liver
42	chr7:137761200-137762000	Active TSS	Liver	Liver
43	chr7:137761200-137763600	Enhancers	HepG2	liver
44	chr7:137762000-137765000	Flanking Active TSS	Liver	Liver
45	chr7:137762400-137762600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:137762400-137763000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:137762400-137763000	Enhancers	HMEC	breast
48	chr7:137762400-137763600	Enhancers	Hela-S3	cervix
49	chr7:137762600-137763000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:137765000-137767000	Enhancers	Liver	Liver

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