Variant report

Variant	nsv1017305
Chromosome Location	chr7:110355786-110382065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:110360293-110360294	K562	blood:	n/a	n/a
2	CTCF	chr7:110373320-110373470	HMEC	breast:	n/a	n/a
3	CTCF	chr7:110373123-110373150	Lung_OC	lung:	n/a	n/a
4	CTCF	chr7:110357254-110357353	Fibrobl	skin:	n/a	n/a
5	CTCF	chr7:110359010-110359062	HepG2	liver:	n/a	n/a
6	CTCF	chr7:110371480-110371630	MCF-7	breast:	n/a	n/a
7	CTCF	chr7:110358940-110359090	BE2_C	brain:	n/a	n/a
8	CTCF	chr7:110373280-110373430	HMEC	breast:	n/a	n/a
9	EBF1	chr7:110360410-110360666	GM12878	blood:	n/a	chr7:110360524-110360534 chr7:110360524-110360533
10	EP300	chr7:110358503-110359012	H1-hESC	embryonic stem cell:	n/a	n/a
11	GTF2F1	chr7:110358793-110358818	H1-hESC	embryonic stem cell:	n/a	n/a
12	HDAC2	chr7:110358579-110359007	H1-hESC	embryonic stem cell:	n/a	n/a
13	JUND	chr7:110358651-110359376	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAFK	chr7:110361495-110361764	HepG2	liver:	n/a	chr7:110361647-110361661 chr7:110361649-110361660 chr7:110361648-110361664 chr7:110361648-110361659 chr7:110361648-110361659
15	MAX	chr7:110358823-110358972	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAZ	chr7:110356064-110356141	HepG2	liver:	n/a	n/a
17	NANOG	chr7:110358575-110358880	H1-hESC	embryonic stem cell:	n/a	n/a
18	NANOG	chr7:110358570-110358977	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr7:110364731-110365345	H1-neurons	neurons:	n/a	n/a
20	POLR2A	chr7:110367338-110367402	MCF-7	breast:	n/a	n/a
21	POLR2A	chr7:110371711-110371776	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr7:110364803-110365383	H1-neurons	neurons:	n/a	n/a
23	POU5F1	chr7:110358498-110358882	H1-hESC	embryonic stem cell:	n/a	n/a
24	RAD21	chr7:110358583-110359111	H1-hESC	embryonic stem cell:	n/a	chr7:110358883-110358897
25	RAD21	chr7:110377412-110377818	H1-hESC	embryonic stem cell:	n/a	n/a
26	RAD21	chr7:110377478-110377688	H1-hESC	embryonic stem cell:	n/a	n/a
27	RAD21	chr7:110358575-110358848	H1-hESC	embryonic stem cell:	n/a	n/a
28	RAD21	chr7:110358860-110359107	SK-N-SH_RA	brain:	n/a	chr7:110358883-110358897
29	RAD21	chr7:110358884-110359105	SK-N-SH_RA	brain:	n/a	n/a
30	RAD21	chr7:110358523-110358965	H1-hESC	embryonic stem cell:	n/a	chr7:110358883-110358897
31	RCOR1	chr7:110365080-110365252	K562	blood:	n/a	n/a
32	STAT3	chr7:110365342-110365359	MCF10A-Er-Src	breast:	n/a	n/a
33	STAT3	chr7:110374373-110374382	MCF10A-Er-Src	breast:	n/a	n/a
34	YY1	chr7:110358606-110358929	H1-hESC	embryonic stem cell:	n/a	n/a
35	ZNF143	chr7:110358565-110358983	H1-hESC	embryonic stem cell:	n/a	n/a
36	ZNF384	chr7:110373369-110373370	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110358708-110358758	GM06990	blood:	n/a
2	chr7:110358708-110358758	T-47D	breast:	n/a
3	chr7:110358708-110358758	SK-N-MC	brain:	n/a
4	chr7:110358708-110358758	SKMC	muscle:	n/a
5	chr7:110364934-110364984	HIPEpiC	eye:	n/a
6	chr7:110364934-110364984	NH-A	brain:	n/a
7	chr7:110358708-110358758	GM12891	blood:	n/a
8	chr7:110358708-110358758	Hela-S3	cervix:	n/a
9	chr7:110358708-110358758	HAEpiC	amniotic membrane:	n/a
10	chr7:110364934-110364984	SK-N-SH	brain:	n/a
11	chr7:110364934-110364984	HEEpiC	esophagus:	n/a
12	chr7:110364934-110364984	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:110364934-110364984	ECC-1	luminal epithelium:	n/a
14	chr7:110364934-110364984	NHBE	bronchial:	n/a
15	chr7:110358708-110358758	NHDF-neo	bronchial:	n/a
16	chr7:110358708-110358758	HIPEpiC	eye:	n/a
17	chr7:110358708-110358758	HEK293	kidney:	embryo
18	chr7:110364934-110364984	HepG2	liver:	n/a
19	chr7:110364934-110364984	MCF10A-Er-Src	breast:	n/a
20	chr7:110358708-110358758	A549	lung:	n/a
21	chr7:110364934-110364984	Caco-2	colon:	n/a
22	chr7:110364934-110364984	A549	lung:	n/a
23	chr7:110358708-110358758	Caco-2	colon:	n/a
24	chr7:110364934-110364984	NHDF-neo	bronchial:	n/a
25	chr7:110364934-110364984	HEK293	kidney:	embryo
26	chr7:110364934-110364984	LNCaP	prostate:	n/a
27	chr7:110364934-110364984	PANC-1	pancreas:	n/a
28	chr7:110358708-110358758	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:110358708-110358758	HCPEpiC	choroid plexus:	n/a
30	chr7:110364934-110364984	K562	blood:	n/a
31	chr7:110358708-110358758	HCF	heart:	n/a
32	chr7:110358708-110358758	U87	brain:	n/a
33	chr7:110364934-110364984	HL-60	blood:	n/a
34	chr7:110364934-110364984	AG09309	skin:	n/a
35	chr7:110358708-110358758	NB4	blood:	n/a
36	chr7:110358708-110358758	BE2_C	brain:	n/a
37	chr7:110358708-110358758	HRCEpiC	kidney:	n/a
38	chr7:110358708-110358758	GM12892	blood:	n/a
39	chr7:110364934-110364984	NB4	blood:	n/a
40	chr7:110364934-110364984	BJ	skin:	n/a
41	chr7:110358708-110358758	Hepatocyte	liver:	n/a
42	chr7:110358708-110358758	AG04449	skin:	fetal
43	chr7:110358708-110358758	Jurkat	blood:	n/a
44	chr7:110358708-110358758	MCF10A-Er-Src	breast:	n/a
45	chr7:110358708-110358758	HepG2	liver:	n/a
46	chr7:110358708-110358758	SAEC	small airway:	n/a
47	chr7:110364934-110364984	NT2-D1	testis:	n/a
48	chr7:110358708-110358758	HCT-116	colon:	n/a
49	chr7:110358708-110358758	HRE	kidney:	n/a
50	chr7:110364934-110364984	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:110355632..110358711-chr7:110362366..110364869,3	K562	blood:
2	chr7:110357101..110359141-chr7:110411715..110414303,2	K562	blood:
3	chr7:110355632..110358711-chr7:110362366..110364869,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-2	chr7:110364215-110364647	ENSG00000228540.1
2	lnc-DOCK4-2	chr7:110365758-110365881	ENSG00000228540.1

No data

Variant related genes	Relation type
ENSG00000228540	TF binding region
ENSG00000228540	CpG island

Extended variants
information (count: 530 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1589883	chr7:110355786-110355787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537161605	chr7:110355800-110355801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143492097	chr7:110355802-110355803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76331983	chr7:110355808-110355809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547601918	chr7:110355833-110355834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1589882	chr7:110355841-110355842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs146745202	chr7:110355929-110355930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4349920	chr7:110355935-110355936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370082873	chr7:110355963-110355964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556148136	chr7:110355965-110355966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575904487	chr7:110355995-110355996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538561871	chr7:110356055-110356056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558704107	chr7:110356065-110356066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35305640	chr7:110356089-110356090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191327120	chr7:110356092-110356093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541119378	chr7:110356093-110356094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184238381	chr7:110356122-110356123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557775232	chr7:110356142-110356143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367848142	chr7:110356150-110356151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189416345	chr7:110356170-110356171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543393632	chr7:110356183-110356184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376564940	chr7:110356197-110356198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529765773	chr7:110356218-110356219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532569507	chr7:110356219-110356220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34160329	chr7:110356259-110356260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369664728	chr7:110356283-110356284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372763710	chr7:110356284-110356285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551819954	chr7:110356286-110356287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12705731	chr7:110356357-110356358	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs527925621	chr7:110356366-110356367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547859973	chr7:110356377-110356378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567381915	chr7:110356393-110356394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536369168	chr7:110356401-110356402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549730671	chr7:110356402-110356403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547980118	chr7:110356412-110356413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12705732	chr7:110356445-110356446	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs149873077	chr7:110356459-110356460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144967732	chr7:110356461-110356462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10260203	chr7:110356463-110356464	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs554754885	chr7:110356484-110356485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574554472	chr7:110356571-110356572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543556110	chr7:110356654-110356655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578024197	chr7:110356685-110356686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77511445	chr7:110356690-110356691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181918377	chr7:110356730-110356731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538911405	chr7:110356735-110356736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545679397	chr7:110356804-110356805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565479348	chr7:110356807-110356808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376861899	chr7:110356850-110356851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557216361	chr7:110356908-110356909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110353000-110355800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:110353600-110356400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:110353600-110358800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:110354600-110356200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:110355800-110356400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:110355800-110357000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:110355800-110358400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:110356000-110357200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:110356200-110357000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:110356400-110356600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr7:110356400-110356800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr7:110356400-110357800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:110356600-110357600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:110356800-110358800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:110357000-110357400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:110357000-110357400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:110357200-110357600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr7:110357400-110360800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:110357400-110361000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:110357600-110358200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:110357600-110361000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:110357800-110358400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:110357800-110359200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr7:110357800-110360600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr7:110358000-110360400	Enhancers	Fetal Brain Male	brain
26	chr7:110358200-110358600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr7:110358200-110360000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:110358400-110358800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr7:110358400-110359000	Enhancers	Fetal Heart	heart
30	chr7:110358400-110359200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr7:110358600-110359000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:110358600-110360400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr7:110358800-110359400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr7:110358800-110359400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:110358800-110359400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:110358800-110359800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:110359000-110365000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:110359200-110359400	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr7:110359200-110360800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:110359400-110359600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:110359400-110359800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr7:110359400-110362800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr7:110359600-110360400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:110361200-110361400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:110362800-110363000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr7:110365000-110365200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:110366000-110366200	Enhancers	Placenta	Placenta
48	chr7:110366800-110367000	Enhancers	Placenta	Placenta
49	chr7:110372000-110373200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:110372400-110374200	Enhancers	Fetal Lung	lung

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