Variant report

Variant	nsv879381
Chromosome Location	chr4:69972086-70046930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69981638-69981898	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70018787-70019146	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
5	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
6	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
7	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
8	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
9	BACH1	chr4:70036465-70036545	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:70033076-70033245	K562	blood:	n/a	n/a
11	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
12	BATF	chr4:69988190-69988541	GM12878	blood:	n/a	n/a
13	BATF	chr4:69988219-69988511	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:69984332-69984392	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
16	CBX3	chr4:70033108-70033324	K562	blood:	n/a	n/a
17	CBX3	chr4:70033000-70033366	K562	blood:	n/a	n/a
18	CEBPB	chr4:70018840-70019114	HepG2	liver:	n/a	chr4:70018982-70018993 chr4:70018982-70018995
19	CEBPB	chr4:70019767-70020117	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:69980567-69980672	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
24	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
25	CEBPB	chr4:70019860-70019969	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
27	CEBPD	chr4:70044512-70044940	K562	blood:	n/a	n/a
28	CEBPD	chr4:70045604-70045791	HepG2	liver:	n/a	n/a
29	CREB1	chr4:70033137-70033332	GM12878	blood:	n/a	n/a
30	CREB1	chr4:70033107-70033379	GM12878	blood:	n/a	n/a
31	CREB1	chr4:70045635-70045816	HepG2	liver:	n/a	n/a
32	CTCF	chr4:70036301-70036515	ECC-1	luminal epithelium:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
33	CTCF	chr4:70022700-70022850	GM12874	blood:	n/a	n/a
34	CTCF	chr4:70036360-70036510	GM12875	blood:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
35	CTCF	chr4:70022780-70022930	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr4:70036293-70036587	K562	blood:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
37	CTCF	chr4:70022830-70022877	A549	lung:	n/a	n/a
38	CTCF	chr4:70022660-70022916	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:70036340-70036490	K562	blood:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
40	CTCF	chr4:70036313-70036547	SK-N-SH_RA	brain:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
41	CTCF	chr4:70036360-70036510	HRPEpiC	eye:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
42	CTCF	chr4:70036300-70036450	HMEC	breast:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
43	CTCF	chr4:70036300-70036545	GM10248	blood:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
44	CTCF	chr4:70022736-70022909	ProgFib	skin:	n/a	n/a
45	CTCF	chr4:70036240-70036390	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr4:70036360-70036510	NHEK	skin:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
47	CTCF	chr4:70036229-70036647	SK-N-SH	brain:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
48	CTCF	chr4:70036336-70036526	GM20000	blood:	n/a	chr4:70036404-70036422 chr4:70036399-70036420
49	CTCF	chr4:70022820-70022970	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr4:70022760-70022910	GM12865	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69976406-69976456	HAEpiC	amniotic membrane:	n/a
2	chr4:69976406-69976456	PANC-1	pancreas:	n/a
3	chr4:69976406-69976456	AG09319	gingival:	n/a
4	chr4:69976406-69976456	SK-N-MC	brain:	n/a
5	chr4:69976406-69976456	NT2-D1	testis:	n/a
6	chr4:69976406-69976456	NHDF-neo	bronchial:	n/a
7	chr4:69976406-69976456	GM12892	blood:	n/a
8	chr4:69976406-69976456	HCT-116	colon:	n/a
9	chr4:69976406-69976456	HRCEpiC	kidney:	n/a
10	chr4:69976406-69976456	Hela-S3	cervix:	n/a
11	chr4:69976406-69976456	HUVEC	blood vessel:	n/a
12	chr4:69976406-69976456	Caco-2	colon:	n/a
13	chr4:69976406-69976456	AG04449	skin:	fetal
14	chr4:69976406-69976456	GM06990	blood:	n/a
15	chr4:69976406-69976456	AG04450	lung:	fetal
16	chr4:69976406-69976456	K562	blood:	n/a
17	chr4:69976406-69976456	HL-60	blood:	n/a
18	chr4:69976406-69976456	CMK	blood:	n/a
19	chr4:69976406-69976456	AG09309	skin:	n/a
20	chr4:69976406-69976456	ECC-1	luminal epithelium:	n/a
21	chr4:69976406-69976456	SK-N-SH_RA	brain:	n/a
22	chr4:69976406-69976456	PFSK-1	brain:	n/a
23	chr4:69976406-69976456	T-47D	breast:	n/a
24	chr4:69976406-69976456	HNPCEpiC	eye:	n/a
25	chr4:69976406-69976456	HEK293	kidney:	embryo
26	chr4:69976406-69976456	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:69976406-69976456	HRPEpiC	eye:	n/a
28	chr4:69976406-69976456	U87	brain:	n/a
29	chr4:69976406-69976456	GM19239	blood:	n/a
30	chr4:69976406-69976456	H1-hESC	embryonic stem cell:	embryo
31	chr4:69976406-69976456	ovcar-3	ovarian:	n/a
32	chr4:69976406-69976456	HEEpiC	esophagus:	n/a
33	chr4:69976406-69976456	HCF	heart:	n/a
34	chr4:69976406-69976456	A549	lung:	n/a
35	chr4:69976406-69976456	HRE	kidney:	n/a
36	chr4:69976406-69976456	RPTEC	kidney:	n/a
37	chr4:69976406-69976456	HMEC	breast:	n/a
38	chr4:69976406-69976456	ProgFib	skin:	n/a
39	chr4:69976406-69976456	PrEC	prostate:	n/a
40	chr4:69976406-69976456	LNCaP	prostate:	n/a
41	chr4:69976406-69976456	NH-A	brain:	n/a
42	chr4:69976406-69976456	HepG2	liver:	n/a
43	chr4:69976406-69976456	AoSMC	blood vessel:	n/a
44	chr4:69976406-69976456	NB4	blood:	n/a
45	chr4:69976406-69976456	MCF10A-Er-Src	breast:	n/a
46	chr4:69976406-69976456	SKMC	muscle:	n/a
47	chr4:69976406-69976456	SK-N-SH	brain:	n/a
48	chr4:69976406-69976456	BJ	skin:	n/a
49	chr4:69976406-69976456	HIPEpiC	eye:	n/a
50	chr4:69976406-69976456	SAEC	small airway:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69981403..69984275-chr4:69989733..69991990,2	K562	blood:
2	chr4:69997242..69999000-chr4:70001834..70004061,2	K562	blood:
3	chr4:69997242..69999000-chr4:70001834..70004061,2	K562	blood:
4	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
5	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B7-1	chr4:69990992-69992169	NONHSAT096754

No data

Variant related genes	Relation type
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000250100	TF binding region
ENSG00000251427	TF binding region
ENSG00000251284	TF binding region
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000250100	CpG island
ENSG00000251427	CpG island
ENSG00000251284	CpG island
ENSG00000251284	chromatin interactions

Extended variants
information (count: 2532 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2532 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12513195	chr4:69972086-69972087	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200027796	chr4:69972089-69972090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542960146	chr4:69972169-69972170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374528003	chr4:69972185-69972186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562634487	chr4:69972220-69972221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191735481	chr4:69972239-69972240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551337040	chr4:69972247-69972248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571301224	chr4:69972248-69972249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4541594	chr4:69972272-69972273	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111852299	chr4:69972307-69972308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4351080	chr4:69972319-69972320	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs184038850	chr4:69972359-69972360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188771998	chr4:69972361-69972362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138334303	chr4:69972390-69972391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4356974	chr4:69972414-69972415	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549502930	chr4:69972419-69972420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543356612	chr4:69972442-69972443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4356975	chr4:69972463-69972464	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
19	rs558102129	chr4:69972487-69972488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578032405	chr4:69972490-69972491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540752993	chr4:69972524-69972525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554175079	chr4:69972548-69972549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111541856	chr4:69972570-69972571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5859161	chr4:69972577-69972578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574093788	chr4:69972608-69972609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143789825	chr4:69972609-69972610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562770571	chr4:69972627-69972628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75446752	chr4:69972632-69972633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181448385	chr4:69972633-69972634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535061824	chr4:69972685-69972686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564952049	chr4:69972689-69972690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527344300	chr4:69972713-69972714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs5013211	chr4:69972777-69972778	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4257713	chr4:69972779-69972780	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377172444	chr4:69972863-69972864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186130517	chr4:69972876-69972877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549405917	chr4:69972884-69972885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569519019	chr4:69972908-69972909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147582860	chr4:69972925-69972926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4292394	chr4:69972949-69972950	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4348159	chr4:69972952-69972953	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs571765031	chr4:69972955-69972956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534247356	chr4:69972956-69972957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371615313	chr4:69972957-69972958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367581820	chr4:69973002-69973003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28365064	chr4:69973042-69973043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4337789	chr4:69973044-69973045	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536641365	chr4:69973059-69973060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7437605	chr4:69973077-69973078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556307486	chr4:69973092-69973093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69959600-69980000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:69963000-69982000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr4:69970000-69980400	Weak transcription	Fetal Intestine Small	intestine
4	chr4:69971000-69981200	Weak transcription	Pancreas	Pancrea
5	chr4:69971400-69981400	Weak transcription	HepG2	liver
6	chr4:69972000-69980400	Strong transcription	Liver	Liver
7	chr4:69973800-69974000	Enhancers	Gastric	stomach
8	chr4:69980000-69981600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:69980400-69980600	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr4:69980400-69982800	Weak transcription	Liver	Liver
11	chr4:69980600-69981400	Weak transcription	Fetal Intestine Small	intestine
12	chr4:69981200-69981600	Enhancers	Pancreas	Pancrea
13	chr4:69981400-69981600	Enhancers	Gastric	stomach
14	chr4:69981400-69982000	Enhancers	Fetal Intestine Large	intestine
15	chr4:69981400-69982200	Enhancers	Fetal Intestine Small	intestine
16	chr4:69981400-69982800	Enhancers	HepG2	liver
17	chr4:69981600-69982600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:69981600-69990800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:69981800-69982800	Weak transcription	Gastric	stomach
20	chr4:69982000-69982800	Active TSS	Fetal Intestine Large	intestine
21	chr4:69982000-69982800	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr4:69982000-69983000	Active TSS	Rectal Mucosa Donor 31	rectum
23	chr4:69982000-69983200	Active TSS	Duodenum Mucosa	Duodenum
24	chr4:69982200-69982400	Flanking Active TSS	Fetal Intestine Small	intestine
25	chr4:69982400-69982800	Active TSS	Fetal Intestine Small	intestine
26	chr4:69982600-69983000	Active TSS	Hela-S3	cervix
27	chr4:69982800-69983000	Enhancers	Liver	Liver
28	chr4:69982800-69983000	Flanking Active TSS	Fetal Intestine Large	intestine
29	chr4:69982800-69983000	Flanking Active TSS	Fetal Intestine Small	intestine
30	chr4:69982800-69983000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr4:69983000-69986200	Weak transcription	Fetal Intestine Small	intestine
32	chr4:69986200-69986400	Enhancers	NHEK	skin
33	chr4:69986200-69987200	Enhancers	Fetal Intestine Small	intestine
34	chr4:69986400-69989800	Weak transcription	NHEK	skin
35	chr4:69986600-69987000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:69986800-69987000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:69987000-69988400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:69987200-69988200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:69987200-69988200	Weak transcription	Fetal Intestine Small	intestine
40	chr4:69987800-69990600	Weak transcription	Gastric	stomach
41	chr4:69988200-69988600	Enhancers	Fetal Intestine Small	intestine
42	chr4:69988200-69989400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:69988400-69988800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:69988800-69989800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:69989400-69990600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:69989800-69991200	Enhancers	NHEK	skin
47	chr4:69989800-69991600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:69990600-69990800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:69990600-69990800	Enhancers	Gastric	stomach
50	chr4:69990600-69990800	Enhancers	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links