Variant report

Variant	nsv1007607
Chromosome Location	chr3:134131521-134156814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:124)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:134146383-134146899	HepG2	liver:	n/a	n/a
2	BCL3	chr3:134145957-134146759	A549	lung:	n/a	chr3:134146368-134146377
3	BCL3	chr3:134146168-134146720	A549	lung:	n/a	chr3:134146368-134146377
4	BHLHE40	chr3:134145816-134146734	HepG2	liver:	n/a	n/a
5	BHLHE40	chr3:134144748-134145112	HepG2	liver:	n/a	n/a
6	BHLHE40	chr3:134146285-134146447	K562	blood:	n/a	n/a
7	BHLHE40	chr3:134138312-134138950	HepG2	liver:	n/a	n/a
8	BHLHE40	chr3:134146104-134146559	A549	lung:	n/a	n/a
9	BRCA1	chr3:134146473-134146649	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:134146237-134146679	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:134146042-134146761	Hela-S3	cervix:	n/a	chr3:134146628-134146639
12	CEBPB	chr3:134150198-134150457	A549	lung:	n/a	chr3:134150352-134150363
13	CEBPB	chr3:134150238-134150499	HepG2	liver:	n/a	chr3:134150352-134150363
14	CEBPB	chr3:134145562-134146811	IMR90	lung:	n/a	chr3:134146628-134146639
15	CEBPB	chr3:134146297-134146691	A549	lung:	n/a	chr3:134146628-134146639
16	CEBPB	chr3:134146133-134146883	A549	lung:	n/a	chr3:134146628-134146639
17	CEBPB	chr3:134146374-134146720	A549	lung:	n/a	chr3:134146628-134146639
18	CEBPB	chr3:134150061-134150566	IMR90	lung:	n/a	chr3:134150352-134150363
19	CEBPB	chr3:134152520-134152701	HepG2	liver:	n/a	chr3:134152662-134152673
20	CEBPB	chr3:134146420-134146819	HepG2	liver:	n/a	chr3:134146628-134146639
21	CEBPB	chr3:134138493-134138840	HepG2	liver:	n/a	n/a
22	CHD1	chr3:134144674-134148152	IMR90	lung:	n/a	n/a
23	CHD2	chr3:134138505-134138940	HepG2	liver:	n/a	n/a
24	CHD2	chr3:134146122-134146742	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr3:134146229-134146835	HepG2	liver:	n/a	n/a
26	CREB1	chr3:134146165-134146575	A549	lung:	n/a	n/a
27	CREB1	chr3:134146236-134146554	A549	lung:	n/a	n/a
28	CTCF	chr3:134146480-134146630	HMEC	breast:	n/a	n/a
29	CTCF	chr3:134146460-134146610	AG09309	skin:	n/a	n/a
30	CTCF	chr3:134146460-134146610	AG09319	gingival:	n/a	n/a
31	CTCF	chr3:134146480-134146630	SAEC	small airway:	n/a	n/a
32	CTCF	chr3:134146439-134146609	NHEK	skin:	n/a	n/a
33	CTCF	chr3:134146360-134146510	NHEK	skin:	n/a	n/a
34	CTCF	chr3:134146460-134146610	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr3:134146360-134146510	HCM	heart:	n/a	n/a
36	CTCF	chr3:134146300-134146450	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr3:134146440-134146590	SAEC	small airway:	n/a	n/a
38	CTCF	chr3:134138531-134138591	GM13976	blood:	n/a	n/a
39	CTCF	chr3:134146460-134146610	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr3:134145422-134145474	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr3:134146420-134146570	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:134146460-134146610	AG04449	skin:	n/a	n/a
43	CTCF	chr3:134146400-134146550	HAc	cerebellar:	n/a	n/a
44	CTCF	chr3:134146480-134146630	AG10803	skin:	n/a	n/a
45	CTCF	chr3:134146365-134146728	IMR90	lung:	n/a	n/a
46	CTCF	chr3:134145320-134145470	AG04449	skin:	n/a	n/a
47	CTCF	chr3:134146460-134146610	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr3:134146480-134146630	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr3:134145420-134145570	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr3:134134943-134134979	Fibrobl	skin:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:134149264-134149314	U87	brain:	n/a
2	chr3:134149264-134149314	H1-hESC	embryonic stem cell:	embryo
3	chr3:134149264-134149314	U87	brain:	n/a
4	chr3:134149264-134149314	H1-hESC	embryonic stem cell:	embryo
5	chr3:134146405-134146455	AoSMC	blood vessel:	n/a
6	chr3:134149264-134149314	RPTEC	kidney:	n/a
7	chr3:134149264-134149314	HMEC	breast:	n/a
8	chr3:134146405-134146455	HAEpiC	amniotic membrane:	n/a
9	chr3:134149264-134149314	HRE	kidney:	n/a
10	chr3:134149264-134149314	SK-N-SH	brain:	n/a
11	chr3:134149264-134149314	IMR90	lung:	fetal
12	chr3:134146405-134146455	HepG2	liver:	n/a
13	chr3:134146405-134146455	K562	blood:	n/a
14	chr3:134146405-134146455	NHBE	bronchial:	n/a
15	chr3:134146405-134146455	NH-A	brain:	n/a
16	chr3:134146405-134146455	HEEpiC	esophagus:	n/a
17	chr3:134149264-134149314	PFSK-1	brain:	n/a
18	chr3:134146405-134146455	GM12878	blood:	n/a
19	chr3:134149264-134149314	HCPEpiC	choroid plexus:	n/a
20	chr3:134149264-134149314	HNPCEpiC	eye:	n/a
21	chr3:134149264-134149314	HL-60	blood:	n/a
22	chr3:134146405-134146455	HCF	heart:	n/a
23	chr3:134146405-134146455	AG10803	skin:	n/a
24	chr3:134149264-134149314	CMK	blood:	n/a
25	chr3:134149264-134149314	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:134146405-134146455	GM12892	blood:	n/a
27	chr3:134146405-134146455	Hela-S3	cervix:	n/a
28	chr3:134149264-134149314	PrEC	prostate:	n/a
29	chr3:134149264-134149314	NB4	blood:	n/a
30	chr3:134146405-134146455	ECC-1	luminal epithelium:	n/a
31	chr3:134149264-134149314	NH-A	brain:	n/a
32	chr3:134149264-134149314	AoSMC	blood vessel:	n/a
33	chr3:134149264-134149314	NT2-D1	testis:	n/a
34	chr3:134146405-134146455	GM12891	blood:	n/a
35	chr3:134146405-134146455	MCF10A-Er-Src	breast:	n/a
36	chr3:134149264-134149314	NHBE	bronchial:	n/a
37	chr3:134149264-134149314	GM12878	blood:	n/a
38	chr3:134146405-134146455	A549	lung:	n/a
39	chr3:134149264-134149314	Jurkat	blood:	n/a
40	chr3:134149264-134149314	AG10803	skin:	n/a
41	chr3:134146405-134146455	MCF-7	breast:	n/a
42	chr3:134149264-134149314	SK-N-SH_RA	brain:	n/a
43	chr3:134149264-134149314	Hela-S3	cervix:	n/a
44	chr3:134149264-134149314	SAEC	small airway:	n/a
45	chr3:134149264-134149314	ovcar-3	ovarian:	n/a
46	chr3:134149264-134149314	HEK293	kidney:	embryo
47	chr3:134146405-134146455	ovcar-3	ovarian:	n/a
48	chr3:134146405-134146455	IMR90	lung:	fetal
49	chr3:134146405-134146455	H1-hESC	embryonic stem cell:	embryo
50	chr3:134149264-134149314	GM19239	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:134029018..134030767-chr3:134154072..134156280,2	MCF-7	breast:
2	chr3:134139549..134143630-chr3:134144649..134147393,5	MCF-7	breast:
3	chr3:134145112..134147635-chr3:134150719..134152522,2	MCF-7	breast:
4	chr3:134146261..134149924-chr3:134150087..134151982,3	MCF-7	breast:
5	chr3:134139570..134141496-chr3:134150691..134153669,2	MCF-7	breast:
6	chr3:134085029..134086901-chr3:134129993..134132969,2	MCF-7	breast:
7	chr3:134145112..134147635-chr3:134150719..134152522,2	MCF-7	breast:
8	chr3:134091888..134095593-chr3:134142304..134147270,4	MCF-7	breast:
9	chr17:56707823..56710437-chr3:134140925..134142745,2	MCF-7	breast:
10	chr3:134129842..134132806-chr3:134133174..134134737,2	MCF-7	breast:
11	chr3:134135737..134137586-chr3:134138996..134140649,2	MCF-7	breast:
12	chr3:134129842..134132806-chr3:134133174..134134737,2	MCF-7	breast:
13	chr3:134148507..134150740-chr3:134203396..134205835,2	K562	blood:
14	chr3:134147507..134149518-chr3:134176090..134178859,2	MCF-7	breast:
15	chr3:134139549..134143630-chr3:134144649..134147393,5	MCF-7	breast:
16	chr3:134137781..134139924-chr3:134140721..134142548,2	MCF-7	breast:
17	chr3:134110212..134112141-chr3:134146148..134148218,2	MCF-7	breast:
18	chr3:134139570..134141496-chr3:134150691..134153669,2	MCF-7	breast:
19	chr3:134044455..134047309-chr3:134153979..134155678,2	MCF-7	breast:
20	chr3:134137781..134139924-chr3:134140721..134142548,2	MCF-7	breast:
21	chr3:134135737..134137586-chr3:134138996..134140649,2	MCF-7	breast:
22	chr3:134146261..134149924-chr3:134150087..134151982,3	MCF-7	breast:
23	chr3:134091106..134093623-chr3:134149755..134152847,3	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4788	chr3:134156678-134156699	MIMAT0019958

No data

Variant related genes	Relation type
MIR4788	TF binding region
HMGB3P13	TF binding region
ENSG00000221313	TF binding region
MIR4788	CpG island
HMGB3P13	CpG island
ENSG00000221313	CpG island
ENSG00000114019	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000129055	chromatin interactions
ENSG00000182923	chromatin interactions

Extended variants
information (count: 1036 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574772618	chr3:134131524-134131525	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs192107787	chr3:134131532-134131533	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547029622	chr3:134131549-134131550	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74866808	chr3:134131588-134131589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543559767	chr3:134131618-134131619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555451650	chr3:134131649-134131650	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569241910	chr3:134131662-134131663	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs142589422	chr3:134131693-134131694	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538113571	chr3:134131705-134131706	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557933987	chr3:134131714-134131715	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs577776669	chr3:134131726-134131727	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs199806946	chr3:134131729-134131730	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368230170	chr3:134131753-134131754	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372935341	chr3:134131783-134131784	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534119255	chr3:134131794-134131795	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs553081924	chr3:134131822-134131823	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572829503	chr3:134131870-134131871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376983584	chr3:134131875-134131876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77956051	chr3:134131882-134131883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184714316	chr3:134131887-134131888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs79971530	chr3:134131894-134131895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201200335	chr3:134131958-134131959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375408508	chr3:134131960-134131961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs202226926	chr3:134131962-134131963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200304452	chr3:134131997-134131998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371679228	chr3:134132005-134132006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374100281	chr3:134132007-134132008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368275316	chr3:134132009-134132010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372564554	chr3:134132011-134132012	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201419780	chr3:134132022-134132023	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545580065	chr3:134132059-134132060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544470835	chr3:134132066-134132067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs377178494	chr3:134132067-134132068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559395762	chr3:134132097-134132098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140094885	chr3:134132115-134132116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35602921	chr3:134132118-134132119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371416857	chr3:134132160-134132161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34941750	chr3:134132161-134132162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561022443	chr3:134132163-134132164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs71624046	chr3:134132199-134132200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10587242	chr3:134132200-134132201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145514247	chr3:134132206-134132207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546475027	chr3:134132274-134132275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187083203	chr3:134132279-134132280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562163781	chr3:134132314-134132315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77673410	chr3:134132366-134132367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199893026	chr3:134132371-134132372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10433422	chr3:134132372-134132373	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568882762	chr3:134132373-134132374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117869694	chr3:134132407-134132408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134126400-134141800	Weak transcription	Brain Angular Gyrus	brain
2	chr3:134126400-134146000	Weak transcription	Pancreas	Pancrea
3	chr3:134129600-134138200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:134133400-134133600	Bivalent Enhancer	Left Ventricle	heart
5	chr3:134137600-134138200	Enhancers	HepG2	liver
6	chr3:134137800-134139400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:134138200-134138400	Enhancers	Colonic Mucosa	Colon
8	chr3:134138200-134138600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr3:134138200-134139000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
10	chr3:134138200-134139000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:134138200-134139000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:134138200-134139200	Flanking Active TSS	HepG2	liver
13	chr3:134138200-134139400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:134138400-134138600	Flanking Active TSS	Colonic Mucosa	Colon
15	chr3:134138400-134138800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:134138400-134138800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:134138400-134138800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:134138400-134138800	Enhancers	Brain Hippocampus Middle	brain
19	chr3:134138400-134139000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:134138400-134139000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr3:134138400-134139000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr3:134138400-134139000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr3:134138400-134139000	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr3:134138400-134139200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:134138400-134139200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:134138400-134139200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:134138600-134138800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:134138600-134139000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:134138600-134139200	Enhancers	Fetal Muscle Leg	muscle
30	chr3:134138600-134139400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr3:134138800-134139000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr3:134138800-134139200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr3:134138800-134141600	Weak transcription	Brain Hippocampus Middle	brain
34	chr3:134138800-134141800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:134138800-134142000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:134139000-134141600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:134139000-134141800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:134139000-134142000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr3:134139000-134142200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:134139000-134142200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr3:134139200-134140000	Enhancers	HepG2	liver
42	chr3:134139200-134141800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr3:134139200-134141800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:134139400-134139600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:134139600-134141800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:134140000-134141800	Weak transcription	HepG2	liver
47	chr3:134140600-134141200	Enhancers	Adipose Nuclei	Adipose
48	chr3:134141200-134143200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr3:134141200-134146000	Weak transcription	Adipose Nuclei	Adipose
50	chr3:134141400-134142400	Enhancers	Brain Inferior Temporal Lobe	brain

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