Variant report

Variant	esv3377641
Chromosome Location	chr7:140181549-140190537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140185697-140185852	K562	blood:	n/a	n/a
2	ARID3A	chr7:140188071-140188442	K562	blood:	n/a	n/a
3	ATF1	chr7:140188073-140188434	K562	blood:	n/a	n/a
4	BACH1	chr7:140185767-140185904	K562	blood:	n/a	n/a
5	BACH1	chr7:140185073-140185560	K562	blood:	n/a	n/a
6	BACH1	chr7:140185264-140185985	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:140188143-140188310	K562	blood:	n/a	n/a
8	BATF	chr7:140186510-140186778	GM12878	blood:	n/a	chr7:140186679-140186690
9	BHLHE40	chr7:140188071-140188558	K562	blood:	n/a	n/a
10	BHLHE40	chr7:140185293-140185448	K562	blood:	n/a	n/a
11	BHLHE40	chr7:140184833-140184843	HepG2	liver:	n/a	n/a
12	CBX3	chr7:140187741-140188634	K562	blood:	n/a	n/a
13	CBX3	chr7:140188694-140189191	K562	blood:	n/a	n/a
14	CCNT2	chr7:140188070-140188497	K562	blood:	n/a	n/a
15	CEBPB	chr7:140184967-140185272	K562	blood:	n/a	n/a
16	CEBPB	chr7:140185594-140185763	K562	blood:	n/a	n/a
17	CEBPB	chr7:140185435-140185689	A549	lung:	n/a	n/a
18	CEBPB	chr7:140184951-140185817	Hela-S3	cervix:	n/a	n/a
19	CEBPD	chr7:140187883-140188589	K562	blood:	n/a	n/a
20	CEBPD	chr7:140187876-140188591	K562	blood:	n/a	n/a
21	CHD2	chr7:140185700-140185845	K562	blood:	n/a	n/a
22	CTCF	chr7:140188275-140188299	K562	blood:	n/a	n/a
23	CUX1	chr7:140185772-140185998	K562	blood:	n/a	n/a
24	CUX1	chr7:140188151-140188438	K562	blood:	n/a	n/a
25	E2F4	chr7:140185450-140185752	MCF10A-Er-Src	breast:	n/a	n/a
26	ELF1	chr7:140185492-140185905	K562	blood:	n/a	n/a
27	EP300	chr7:140188251-140188549	GM12878	blood:	n/a	n/a
28	EP300	chr7:140188132-140188382	K562	blood:	n/a	n/a
29	EP300	chr7:140185620-140185886	K562	blood:	n/a	n/a
30	EP300	chr7:140185147-140185346	K562	blood:	n/a	n/a
31	EP300	chr7:140187905-140189131	K562	blood:	n/a	n/a
32	FOS	chr7:140185428-140185693	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr7:140185376-140185810	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr7:140185056-140185850	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr7:140184982-140185811	MCF10A-Er-Src	breast:	n/a	n/a
36	GATA1	chr7:140187818-140189359	K562	blood:	n/a	n/a
37	GATA1	chr7:140187999-140188511	PBDE	blood:	n/a	n/a
38	GATA1	chr7:140188078-140188384	K562	blood:	n/a	n/a
39	GATA2	chr7:140188072-140188465	K562	blood:	n/a	n/a
40	GATA2	chr7:140187932-140188471	K562	blood:	n/a	n/a
41	GATA2	chr7:140187947-140188389	K562	blood:	n/a	n/a
42	GTF2B	chr7:140188364-140188514	K562	blood:	n/a	n/a
43	HDAC2	chr7:140188070-140188358	K562	blood:	n/a	n/a
44	HDAC2	chr7:140187949-140188564	K562	blood:	n/a	n/a
45	HEY1	chr7:140188251-140188597	K562	blood:	n/a	n/a
46	HEY1	chr7:140188014-140188247	K562	blood:	n/a	n/a
47	HMGN3	chr7:140188120-140188336	K562	blood:	n/a	n/a
48	IRF1	chr7:140188026-140188538	K562	blood:	n/a	n/a
49	IRF1	chr7:140188109-140188340	K562	blood:	n/a	n/a
50	IRF1	chr7:140185560-140185577	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140182232-140182282	ECC-1	luminal epithelium:	n/a
2	chr7:140182232-140182282	SKMC	muscle:	n/a
3	chr7:140182232-140182282	HRE	kidney:	n/a
4	chr7:140182232-140182282	RPTEC	kidney:	n/a
5	chr7:140182232-140182282	PFSK-1	brain:	n/a
6	chr7:140182232-140182282	HepG2	liver:	n/a
7	chr7:140182232-140182282	PrEC	prostate:	n/a
8	chr7:140182232-140182282	SK-N-SH	brain:	n/a
9	chr7:140182232-140182282	HIPEpiC	eye:	n/a
10	chr7:140182232-140182282	A549	lung:	n/a
11	chr7:140182232-140182282	HRCEpiC	kidney:	n/a
12	chr7:140182232-140182282	T-47D	breast:	n/a
13	chr7:140182232-140182282	AG04449	skin:	fetal
14	chr7:140182232-140182282	Hela-S3	cervix:	n/a
15	chr7:140182232-140182282	BJ	skin:	n/a
16	chr7:140182232-140182282	HCM	heart:	n/a
17	chr7:140182232-140182282	GM12892	blood:	n/a
18	chr7:140182232-140182282	HNPCEpiC	eye:	n/a
19	chr7:140182232-140182282	HEK293	kidney:	embryo
20	chr7:140182232-140182282	AG10803	skin:	n/a
21	chr7:140182232-140182282	GM12878	blood:	n/a
22	chr7:140182232-140182282	IMR90	lung:	fetal
23	chr7:140182232-140182282	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:140182232-140182282	HMEC	breast:	n/a
25	chr7:140182232-140182282	H1-hESC	embryonic stem cell:	embryo
26	chr7:140182232-140182282	HAEpiC	amniotic membrane:	n/a
27	chr7:140182232-140182282	CMK	blood:	n/a
28	chr7:140182232-140182282	AG09319	gingival:	n/a
29	chr7:140182232-140182282	ovcar-3	ovarian:	n/a
30	chr7:140182232-140182282	Caco-2	colon:	n/a
31	chr7:140182232-140182282	MCF-7	breast:	n/a
32	chr7:140182232-140182282	NHDF-neo	bronchial:	n/a
33	chr7:140182232-140182282	NH-A	brain:	n/a
34	chr7:140182232-140182282	HRPEpiC	eye:	n/a
35	chr7:140182232-140182282	SK-N-MC	brain:	n/a
36	chr7:140182232-140182282	GM06990	blood:	n/a
37	chr7:140182232-140182282	GM12891	blood:	n/a
38	chr7:140182232-140182282	AoSMC	blood vessel:	n/a
39	chr7:140182232-140182282	U87	brain:	n/a
40	chr7:140182232-140182282	K562	blood:	n/a
41	chr7:140182232-140182282	HL-60	blood:	n/a
42	chr7:140182232-140182282	ProgFib	skin:	n/a
43	chr7:140182232-140182282	AG09309	skin:	n/a
44	chr7:140182232-140182282	AG04450	lung:	fetal
45	chr7:140182232-140182282	HCPEpiC	choroid plexus:	n/a
46	chr7:140182232-140182282	LNCaP	prostate:	n/a
47	chr7:140182232-140182282	HEEpiC	esophagus:	n/a
48	chr7:140182232-140182282	NT2-D1	testis:	n/a
49	chr7:140182232-140182282	NB4	blood:	n/a
50	chr7:140182232-140182282	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:140178521..140180888-chr7:140189014..140190989,2	K562	blood:
2	chr7:140177800..140180943-chr7:140182386..140186052,5	MCF-7	breast:
3	chr7:140175927..140181758-chr7:140182392..140187030,7	K562	blood:
4	chr7:140176571..140180021-chr7:140187634..140190989,3	K562	blood:
5	chr7:140188257..140190605-chr7:140190654..140192972,3	K562	blood:
6	chr7:140182169..140184861-chr7:140185042..140187424,2	K562	blood:
7	chr7:140178138..140180332-chr7:140181621..140183452,2	MCF-7	breast:
8	chr7:139875628..139877580-chr7:140184540..140187021,2	K562	blood:
9	chr7:140182169..140184861-chr7:140185042..140187424,2	K562	blood:
10	chr7:140173004..140174685-chr7:140179512..140182205,2	MCF-7	breast:

No data

Variant related genes	Relation type
MKRN1	TF binding region
MKRN1	CpG island
ENSG00000260231	chromatin interactions
ENSG00000133606	chromatin interactions
ENSG00000006459	chromatin interactions

Extended variants
information (count: 409 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565954459	chr7:140181566-140181567	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs532806672	chr7:140181567-140181568	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528140877	chr7:140181589-140181590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs191330556	chr7:140181623-140181624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201790890	chr7:140181642-140181643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561571561	chr7:140181663-140181664	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs570245197	chr7:140181678-140181679	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs537680135	chr7:140181697-140181698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541737712	chr7:140181700-140181701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs71552618	chr7:140181729-140181730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182847920	chr7:140181730-140181731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370315151	chr7:140181732-140181733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs202049304	chr7:140181735-140181736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200340951	chr7:140181740-140181741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571969133	chr7:140181782-140181783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550891112	chr7:140181786-140181787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546057314	chr7:140181793-140181794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564074170	chr7:140181843-140181844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs111506871	chr7:140181871-140181872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs13246753	chr7:140181930-140181931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs111661389	chr7:140181931-140181932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529353872	chr7:140182038-140182039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547595759	chr7:140182054-140182055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375245065	chr7:140182070-140182071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551198606	chr7:140182101-140182102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551767572	chr7:140182146-140182147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533203125	chr7:140182175-140182176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550338387	chr7:140182191-140182192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552091129	chr7:140182209-140182210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139676958	chr7:140182212-140182213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs7799539	chr7:140182213-140182214	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188317398	chr7:140182222-140182223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78284791	chr7:140182233-140182234	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs566859032	chr7:140182251-140182252	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs535507540	chr7:140182267-140182268	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377117974	chr7:140182268-140182269	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs7777769	chr7:140182269-140182270	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560029536	chr7:140182303-140182304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368476181	chr7:140182339-140182340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7785094	chr7:140182402-140182403	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs375494486	chr7:140182422-140182423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575891358	chr7:140182434-140182435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368494374	chr7:140182471-140182472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144364759	chr7:140182495-140182496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146613136	chr7:140182506-140182507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113247159	chr7:140182514-140182515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559629210	chr7:140182545-140182546	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533355627	chr7:140182557-140182558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551755460	chr7:140182566-140182567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563684573	chr7:140182575-140182576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Myelodysplastic syndrome	17634407	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
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19826477	CNVD
Melanoma	19509136	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140179800-140183000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:140179800-140183400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:140179800-140183400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:140179800-140184400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:140179800-140184600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:140179800-140184800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:140179800-140185200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:140179800-140187800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:140179800-140198000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:140180000-140183200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:140180000-140183200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:140180000-140183200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:140180000-140183400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:140180000-140184400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:140180000-140184400	Weak transcription	Fetal Intestine Large	intestine
16	chr7:140180000-140184400	Weak transcription	Fetal Intestine Small	intestine
17	chr7:140180000-140184400	Weak transcription	Hela-S3	cervix
18	chr7:140180000-140184400	Weak transcription	K562	blood
19	chr7:140180000-140184600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:140180000-140184600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:140180000-140184600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:140180000-140184800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:140180000-140184800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:140180000-140184800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr7:140180000-140185200	Weak transcription	NHEK	skin
26	chr7:140180000-140188200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:140181200-140181600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr7:140181200-140181600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:140181200-140181600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr7:140181400-140181600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:140181400-140183200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr7:140181600-140182200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:140181600-140183200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr7:140181600-140183200	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr7:140181600-140183200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr7:140182200-140184600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:140183000-140185800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:140183200-140183600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:140183200-140183800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:140183200-140184600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:140183200-140184600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:140183200-140184600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:140183200-140185200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:140183200-140185200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr7:140183400-140184600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:140183400-140185200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr7:140183400-140185800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:140183600-140184400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:140183800-140184200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:140184200-140184600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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