Variant report

Variant	nsv516703
Chromosome Location	chr3:113560020-113615243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:488)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:113563487-113563843	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:113592645-113593092	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:113613793-113614046	HepG2	liver:	n/a	n/a
4	BHLHE40	chr3:113563537-113563769	GM12878	blood:	n/a	n/a
5	CBX3	chr3:113598730-113599055	K562	blood:	n/a	n/a
6	CEBPB	chr3:113566786-113567374	MCF-7	breast:	n/a	n/a
7	CEBPB	chr3:113566853-113567372	HCT-116	colon:	n/a	n/a
8	CEBPB	chr3:113566962-113567383	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr3:113566783-113567371	HCT-116	colon:	n/a	n/a
10	CEBPB	chr3:113566999-113567271	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:113592722-113593062	HepG2	liver:	n/a	chr3:113592898-113592909 chr3:113592919-113592930
12	CEBPB	chr3:113566855-113567338	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr3:113566941-113567255	A549	lung:	n/a	n/a
14	CEBPB	chr3:113567006-113567155	K562	blood:	n/a	n/a
15	CEBPB	chr3:113583765-113584065	HepG2	liver:	n/a	chr3:113583925-113583936
16	CEBPB	chr3:113609114-113609530	MCF-7	breast:	n/a	n/a
17	CEBPB	chr3:113583800-113584036	A549	lung:	n/a	chr3:113583925-113583936
18	CEBPB	chr3:113576517-113576704	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:113566842-113567355	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:113566882-113567369	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:113563571-113563759	GM13977	blood:	n/a	n/a
22	CTCF	chr3:113563600-113563750	GM12865	blood:	n/a	n/a
23	CTCF	chr3:113563600-113563750	GM06990	blood:	n/a	n/a
24	CTCF	chr3:113582540-113582690	HepG2	liver:	n/a	n/a
25	CTCF	chr3:113563580-113563730	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr3:113609220-113609370	SAEC	small airway:	n/a	n/a
27	CTCF	chr3:113569146-113569238	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:113563560-113563710	GM12866	blood:	n/a	n/a
29	CTCF	chr3:113563600-113563750	NB4	blood:	n/a	n/a
30	CTCF	chr3:113609160-113609310	GM12873	blood:	n/a	n/a
31	CTCF	chr3:113563560-113563710	BJ	skin:	n/a	n/a
32	CTCF	chr3:113563565-113563847	A549	lung:	n/a	n/a
33	CTCF	chr3:113563560-113563710	GM12873	blood:	n/a	n/a
34	CTCF	chr3:113563504-113563935	HCT-116	colon:	n/a	n/a
35	CTCF	chr3:113563620-113563770	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr3:113569155-113569200	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:113609280-113609430	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:113563600-113563750	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr3:113563680-113563830	HAc	cerebellar:	n/a	n/a
40	CTCF	chr3:113563600-113563750	AG10803	skin:	n/a	n/a
41	CTCF	chr3:113563680-113563830	HFF	foreskin:	n/a	n/a
42	CTCF	chr3:113563580-113563730	RPTEC	kidney:	n/a	n/a
43	CTCF	chr3:113563620-113563770	GM12867	blood:	n/a	n/a
44	CTCF	chr3:113609164-113609451	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:113609200-113609406	GM12892	blood:	n/a	n/a
46	CTCF	chr3:113563540-113563690	HCT-116	colon:	n/a	n/a
47	CTCF	chr3:113609225-113609400	K562	blood:	n/a	n/a
48	CTCF	chr3:113609235-113609417	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr3:113563560-113563710	HVMF	connective:	n/a	n/a
50	CTCF	chr3:113609220-113609370	HCT-116	colon:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:113560972-113561022	SK-N-SH_RA	brain:	n/a
2	chr3:113560972-113561022	HCT-116	colon:	n/a
3	chr3:113603874-113603924	BJ	skin:	n/a
4	chr3:113604392-113604442	AG10803	skin:	n/a
5	chr3:113604183-113604233	ovcar-3	ovarian:	n/a
6	chr3:113604241-113604291	HRPEpiC	eye:	n/a
7	chr3:113560972-113561022	K562	blood:	n/a
8	chr3:113604392-113604442	HMEC	breast:	n/a
9	chr3:113606269-113606319	PFSK-1	brain:	n/a
10	chr3:113560972-113561022	HMEC	breast:	n/a
11	chr3:113604392-113604442	GM12891	blood:	n/a
12	chr3:113603874-113603924	U87	brain:	n/a
13	chr3:113604241-113604291	AG04449	skin:	fetal
14	chr3:113604241-113604291	AG04450	lung:	fetal
15	chr3:113602333-113602383	Hepatocyte	liver:	n/a
16	chr3:113606269-113606319	HEEpiC	esophagus:	n/a
17	chr3:113599916-113599966	HNPCEpiC	eye:	n/a
18	chr3:113604241-113604291	HRCEpiC	kidney:	n/a
19	chr3:113604392-113604442	SAEC	small airway:	n/a
20	chr3:113603874-113603924	HCPEpiC	choroid plexus:	n/a
21	chr3:113604392-113604442	NHBE	bronchial:	n/a
22	chr3:113604392-113604442	GM19239	blood:	n/a
23	chr3:113560972-113561022	GM12891	blood:	n/a
24	chr3:113602333-113602383	NHDF-neo	bronchial:	n/a
25	chr3:113599916-113599966	AG10803	skin:	n/a
26	chr3:113602333-113602383	H1-hESC	embryonic stem cell:	embryo
27	chr3:113602333-113602383	SAEC	small airway:	n/a
28	chr3:113604183-113604233	HCPEpiC	choroid plexus:	n/a
29	chr3:113604183-113604233	SKMC	muscle:	n/a
30	chr3:113604183-113604233	HRPEpiC	eye:	n/a
31	chr3:113604183-113604233	GM12892	blood:	n/a
32	chr3:113599916-113599966	NHDF-neo	bronchial:	n/a
33	chr3:113602333-113602383	NH-A	brain:	n/a
34	chr3:113602333-113602383	K562	blood:	n/a
35	chr3:113560972-113561022	LNCaP	prostate:	n/a
36	chr3:113602333-113602383	AG04450	lung:	fetal
37	chr3:113560972-113561022	BE2_C	brain:	n/a
38	chr3:113604392-113604442	HEK293	kidney:	embryo
39	chr3:113604183-113604233	HepG2	liver:	n/a
40	chr3:113603874-113603924	SAEC	small airway:	n/a
41	chr3:113602333-113602383	HCT-116	colon:	n/a
42	chr3:113604183-113604233	AG04449	skin:	fetal
43	chr3:113560972-113561022	HAEpiC	amniotic membrane:	n/a
44	chr3:113602333-113602383	AG09309	skin:	n/a
45	chr3:113604241-113604291	SKMC	muscle:	n/a
46	chr3:113602333-113602383	MCF10A-Er-Src	breast:	n/a
47	chr3:113604392-113604442	CMK	blood:	n/a
48	chr3:113599916-113599966	CMK	blood:	n/a
49	chr3:113604241-113604291	BE2_C	brain:	n/a
50	chr3:113560972-113561022	SKMC	muscle:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:113558122..113560757-chr3:113561345..113564124,3	K562	blood:
2	chr3:113464701..113467422-chr3:113608653..113611479,2	K562	blood:
3	chr3:113607843..113610621-chr3:113612739..113615522,2	K562	blood:
4	chr3:113612373..113614219-chr3:113615941..113617468,2	MCF-7	breast:
5	chr3:113608263..113610778-chr3:113614290..113616255,2	MCF-7	breast:
6	chr3:113615024..113616556-chr3:113664464..113667228,2	MCF-7	breast:
7	chr3:113563584..113564144-chr3:113631853..113632404,2	MCF-7	breast:
8	chr3:113564891..113567125-chr3:113615091..113617846,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAA50-4	chr3:113569084-113569578	NONHSAT091250
2	lnc-ATP6V1A-2	chr3:113594331-113594714	NONHSAT091246
3	lnc-ATP6V1A-2	chr3:113563670-113563812	NONHSAT091249
4	lnc-ATP6V1A-2	chr3:113563350-113563496	NONHSAT091249
5	lnc-ATP6V1A-2	chr3:113588354-113588438	NONHSAT091246
6	lnc-ATP6V1A-2	chr3:113563350-113563496	NONHSAT091246

No data

Variant related genes	Relation type
ENSG00000240776	TF binding region
GRAMD1C	TF binding region
ENSG00000241889	TF binding region
ENSG00000240776	CpG island
GRAMD1C	CpG island
ENSG00000241889	CpG island
ENSG00000178075	chromatin interactions
ENSG00000121579	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000273394	chromatin interactions
ENSG00000184307	chromatin interactions
ENSG00000242659	chromatin interactions

Extended variants
information (count: 1722 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1722 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2566980	chr3:113560020-113560021	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs578111368	chr3:113560033-113560034	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs151121078	chr3:113560064-113560065	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528345501	chr3:113560068-113560069	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368273057	chr3:113560128-113560129	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115568397	chr3:113560132-113560133	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs373639828	chr3:113560133-113560134	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs56205830	chr3:113560148-113560149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199705837	chr3:113560149-113560150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142598369	chr3:113560210-113560211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540291343	chr3:113560217-113560218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376036786	chr3:113560226-113560227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539166237	chr3:113560232-113560233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs146903289	chr3:113560239-113560240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569475679	chr3:113560273-113560274	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536444694	chr3:113560277-113560278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139078123	chr3:113560289-113560290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573469606	chr3:113560297-113560298	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576673066	chr3:113560328-113560329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534193241	chr3:113560367-113560368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552576900	chr3:113560370-113560371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577202021	chr3:113560394-113560395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115677150	chr3:113560429-113560430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563230452	chr3:113560453-113560454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78889994	chr3:113560479-113560480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs7628645	chr3:113560482-113560483	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs561101455	chr3:113560596-113560597	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs111600092	chr3:113560719-113560720	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149044645	chr3:113560731-113560732	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2712329	chr3:113560744-113560745	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs181618365	chr3:113560752-113560753	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs117961879	chr3:113560822-113560823	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532541720	chr3:113560830-113560831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150436593	chr3:113560886-113560887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149060437	chr3:113560896-113560897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540702661	chr3:113560962-113560963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367930702	chr3:113560965-113560966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577151573	chr3:113561041-113561042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530169736	chr3:113561048-113561049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375223123	chr3:113561127-113561128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369604365	chr3:113561157-113561158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185845084	chr3:113561158-113561159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188718368	chr3:113561320-113561321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115727023	chr3:113561332-113561333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138192171	chr3:113561391-113561392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78271985	chr3:113561398-113561399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558814728	chr3:113561405-113561406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373013157	chr3:113561432-113561433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570953650	chr3:113561489-113561490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2399490	chr3:113561504-113561505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:67)

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
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	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
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113558200-113570800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:113558400-113566400	Weak transcription	Fetal Intestine Small	intestine
3	chr3:113558600-113563800	Weak transcription	Liver	Liver
4	chr3:113558600-113566600	Weak transcription	Fetal Kidney	kidney
5	chr3:113558600-113566600	Weak transcription	NHLF	lung
6	chr3:113558600-113574800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:113558800-113566600	Weak transcription	HUVEC	blood vessel
8	chr3:113559200-113560400	Enhancers	Placenta	Placenta
9	chr3:113559600-113562200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr3:113560400-113566600	Weak transcription	Placenta	Placenta
11	chr3:113562600-113566400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr3:113563800-113564200	Enhancers	Liver	Liver
13	chr3:113564200-113565400	Weak transcription	Liver	Liver
14	chr3:113565000-113566400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr3:113565400-113565600	Enhancers	Fetal Intestine Large	intestine
16	chr3:113565400-113565600	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr3:113565400-113566400	Enhancers	Liver	Liver
18	chr3:113565600-113566400	Weak transcription	Fetal Intestine Large	intestine
19	chr3:113565600-113566400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr3:113566200-113566400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr3:113566200-113567600	Enhancers	Stomach Mucosa	stomach
22	chr3:113566400-113566800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr3:113566400-113566800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr3:113566400-113566800	Enhancers	Small Intestine	intestine
25	chr3:113566400-113567000	Flanking Active TSS	Liver	Liver
26	chr3:113566400-113567200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:113566400-113567600	Enhancers	Duodenum Mucosa	Duodenum
28	chr3:113566400-113567600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr3:113566400-113568000	Enhancers	Fetal Intestine Large	intestine
30	chr3:113566400-113568000	Enhancers	Fetal Intestine Small	intestine
31	chr3:113566600-113566800	Enhancers	Placenta	Placenta
32	chr3:113566600-113566800	Enhancers	HUVEC	blood vessel
33	chr3:113566600-113566800	Enhancers	NHLF	lung
34	chr3:113566600-113567000	Enhancers	Fetal Kidney	kidney
35	chr3:113566600-113567200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr3:113566600-113567200	Enhancers	Hela-S3	cervix
37	chr3:113566600-113567600	Enhancers	HMEC	breast
38	chr3:113566600-113567600	Enhancers	NHEK	skin
39	chr3:113566600-113568000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:113566800-113567000	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr3:113566800-113567400	Weak transcription	Placenta	Placenta
42	chr3:113566800-113571200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr3:113567000-113567600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr3:113567000-113567600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr3:113567000-113568000	Enhancers	Liver	Liver
46	chr3:113567200-113570400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr3:113567400-113567600	Enhancers	Placenta	Placenta
48	chr3:113567600-113569200	Weak transcription	Placenta	Placenta
49	chr3:113568000-113569200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:113568000-113571200	Weak transcription	Fetal Intestine Small	intestine

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