Variant report

Variant	nsv471042
Chromosome Location	chr5:113160490-113440892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:892)
CpG islands
(count:916)
Chromatin interactive
region (count:19)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:892 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:113369231-113369371	K562	blood:	n/a	n/a
2	BACH1	chr5:113425513-113425525	K562	blood:	n/a	n/a
3	BHLHE40	chr5:113230954-113230962	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:113391550-113391615	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr5:113205683-113205718	GM12878	blood:	n/a	n/a
6	CBX3	chr5:113428211-113428375	K562	blood:	n/a	n/a
7	CEBPB	chr5:113315287-113315399	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:113245946-113246198	A549	lung:	n/a	chr5:113246081-113246092
9	CEBPB	chr5:113222517-113222756	HepG2	liver:	n/a	chr5:113222645-113222656
10	CEBPB	chr5:113250393-113250630	HepG2	liver:	n/a	chr5:113250475-113250488
11	CEBPB	chr5:113288756-113288930	A549	lung:	n/a	chr5:113288810-113288821 chr5:113288809-113288822
12	CEBPB	chr5:113244952-113244953	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:113398874-113399149	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:113245954-113246231	HepG2	liver:	n/a	chr5:113246081-113246092
15	CEBPB	chr5:113288714-113288938	IMR90	lung:	n/a	chr5:113288810-113288821 chr5:113288809-113288822
16	CEBPB	chr5:113245961-113246219	IMR90	lung:	n/a	chr5:113246081-113246092
17	CEBPB	chr5:113418529-113418831	IMR90	lung:	n/a	chr5:113418688-113418699
18	CEBPB	chr5:113182636-113183051	MCF-7	breast:	n/a	n/a
19	CEBPB	chr5:113288568-113288944	HepG2	liver:	n/a	chr5:113288810-113288821 chr5:113288809-113288822
20	CEBPB	chr5:113250403-113250618	A549	lung:	n/a	chr5:113250475-113250488
21	CEBPB	chr5:113214023-113214086	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:113418595-113418829	HepG2	liver:	n/a	chr5:113418688-113418699
23	CEBPB	chr5:113418612-113418801	A549	lung:	n/a	chr5:113418688-113418699
24	CEBPB	chr5:113317144-113317386	HepG2	liver:	n/a	chr5:113317303-113317314
25	CHD1	chr5:113391235-113391476	H1-hESC	embryonic stem cell:	n/a	chr5:113391383-113391393
26	CHD2	chr5:113391017-113391736	H1-hESC	embryonic stem cell:	n/a	chr5:113391383-113391393
27	CTBP2	chr5:113390946-113392094	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr5:113391080-113391230	HCM	heart:	n/a	n/a
29	CTCF	chr5:113391060-113391210	AG04449	skin:	n/a	n/a
30	CTCF	chr5:113433360-113433510	GM12874	blood:	n/a	n/a
31	CTCF	chr5:113391040-113391190	WI-38	lung:	n/a	n/a
32	CTCF	chr5:113436797-113437313	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:113437000-113437150	AG09319	gingival:	n/a	n/a
34	CTCF	chr5:113433420-113433570	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr5:113399333-113399401	GM12878	blood:	n/a	chr5:113399365-113399374 chr5:113399362-113399380 chr5:113399364-113399385
36	CTCF	chr5:113437180-113437330	HCT-116	colon:	n/a	n/a
37	CTCF	chr5:113357703-113357844	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:113354140-113354290	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr5:113399400-113399550	HFF	foreskin:	n/a	n/a
40	CTCF	chr5:113439230-113439312	GM13976	blood:	n/a	n/a
41	CTCF	chr5:113353960-113354110	NHDF-neo	bronchial:	n/a	chr5:113354016-113354037 chr5:113354014-113354032
42	CTCF	chr5:113436960-113437110	GM06990	blood:	n/a	n/a
43	CTCF	chr5:113428140-113428290	GM12869	blood:	n/a	n/a
44	CTCF	chr5:113326360-113326510	Caco-2	colon:	n/a	n/a
45	CTCF	chr5:113326260-113326410	HVMF	connective:	n/a	n/a
46	CTCF	chr5:113357720-113357870	HepG2	liver:	n/a	n/a
47	CTCF	chr5:113436957-113437138	ProgFib	skin:	n/a	n/a
48	CTCF	chr5:113195501-113195752	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:113436980-113437130	GM06990	blood:	n/a	n/a
50	CTCF	chr5:113436947-113437156	NHEK	skin:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:113391671-113391721	NHBE	bronchial:	n/a
2	chr5:113391671-113391721	NHBE	bronchial:	n/a
3	chr5:113390882-113390932	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:113391125-113391175	HAEpiC	amniotic membrane:	n/a
5	chr5:113390551-113390601	SK-N-SH_RA	brain:	n/a
6	chr5:113181729-113181779	AoSMC	blood vessel:	n/a
7	chr5:113392004-113392054	SK-N-SH_RA	brain:	n/a
8	chr5:113391280-113391330	SK-N-SH	brain:	n/a
9	chr5:113391294-113391344	AG10803	skin:	n/a
10	chr5:113405727-113405777	HAEpiC	amniotic membrane:	n/a
11	chr5:113392004-113392054	AG10803	skin:	n/a
12	chr5:113390882-113390932	HIPEpiC	eye:	n/a
13	chr5:113388886-113388936	NB4	blood:	n/a
14	chr5:113390882-113390932	GM12891	blood:	n/a
15	chr5:113181729-113181779	HRE	kidney:	n/a
16	chr5:113392117-113392167	U87	brain:	n/a
17	chr5:113181729-113181779	SK-N-MC	brain:	n/a
18	chr5:113391671-113391721	SK-N-SH_RA	brain:	n/a
19	chr5:113391125-113391175	HCT-116	colon:	n/a
20	chr5:113390551-113390601	HUVEC	blood vessel:	n/a
21	chr5:113391339-113391389	NB4	blood:	n/a
22	chr5:113391671-113391721	HCM	heart:	n/a
23	chr5:113391125-113391175	AG10803	skin:	n/a
24	chr5:113390882-113390932	Jurkat	blood:	n/a
25	chr5:113181729-113181779	NHDF-neo	bronchial:	n/a
26	chr5:113388886-113388936	GM12891	blood:	n/a
27	chr5:113394591-113394641	AG04449	skin:	fetal
28	chr5:113392004-113392054	MCF10A-Er-Src	breast:	n/a
29	chr5:113388886-113388936	BJ	skin:	n/a
30	chr5:113391125-113391175	HRPEpiC	eye:	n/a
31	chr5:113388886-113388936	SAEC	small airway:	n/a
32	chr5:113391671-113391721	GM12891	blood:	n/a
33	chr5:113394591-113394641	SK-N-MC	brain:	n/a
34	chr5:113391568-113391618	LNCaP	prostate:	n/a
35	chr5:113391568-113391618	Caco-2	colon:	n/a
36	chr5:113391280-113391330	AG04450	lung:	fetal
37	chr5:113391280-113391330	SK-N-MC	brain:	n/a
38	chr5:113391568-113391618	BJ	skin:	n/a
39	chr5:113390551-113390601	ProgFib	skin:	n/a
40	chr5:113391339-113391389	GM19239	blood:	n/a
41	chr5:113181729-113181779	K562	blood:	n/a
42	chr5:113391671-113391721	Hepatocyte	liver:	n/a
43	chr5:113391774-113391824	AG09319	gingival:	n/a
44	chr5:113391774-113391824	Hepatocyte	liver:	n/a
45	chr5:113181729-113181779	Jurkat	blood:	n/a
46	chr5:113392117-113392167	A549	lung:	n/a
47	chr5:113390551-113390601	HEEpiC	esophagus:	n/a
48	chr5:113394591-113394641	HMEC	breast:	n/a
49	chr5:113390882-113390932	BE2_C	brain:	n/a
50	chr5:113391774-113391824	A549	lung:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:113305896..113307463-chr5:113310563..113313169,2	MCF-7	breast:
2	chr5:113436973..113437523-chr5:113785352..113786179,2	MCF-7	breast:
3	chr5:113195360..113195959-chr5:113641044..113641978,2	MCF-7	breast:
4	chr5:113436580..113437551-chr5:113785684..113786466,3	MCF-7	breast:
5	chr5:113436290..113437547-chr5:113640998..113641653,3	MCF-7	breast:
6	chr5:113274920..113276751-chr5:113279432..113281008,2	MCF-7	breast:
7	chr5:113344460..113347767-chr5:113347834..113352553,4	K562	blood:
8	chr5:113274920..113276751-chr5:113279432..113281008,2	MCF-7	breast:
9	chr5:113286903..113288673-chr5:113295671..113298612,2	MCF-7	breast:
10	chr5:113253610..113254277-chr5:113433047..113433596,2	MCF-7	breast:
11	chr5:113352228..113355124-chr5:113389622..113391214,2	MCF-7	breast:
12	chr5:113286903..113288673-chr5:113295671..113298612,2	MCF-7	breast:
13	chr5:113305896..113307463-chr5:113310563..113313169,2	MCF-7	breast:
14	chr5:113262773..113264942-chr5:113274128..113275756,2	MCF-7	breast:
15	chr5:113344460..113347767-chr5:113347834..113352553,4	K562	blood:
16	chr5:113352228..113355124-chr5:113389622..113391214,2	MCF-7	breast:
17	chr5:113353815..113354481-chr5:113785668..113786271,3	MCF-7	breast:
18	chr5:113253610..113254277-chr5:113433047..113433596,2	MCF-7	breast:
19	chr5:113262773..113264942-chr5:113274128..113275756,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNN2-4	chr5:113419572-113420096	l_2997_chr5:113419571-113469367_heart
2	lnc-KCNN2-2	chr5:113391684-113392197	NONHSAT103275
3	lnc-KCNN2-2	chr5:113391703-113392197	XLOC_004511
4	lnc-KCNN2-2	chr5:113392797-113392869	NONHSAT103275
5	lnc-KCNN2-2	chr5:113392797-113392868	XLOC_004511
6	lnc-KCNN2-2	chr5:113391840-113392197	XLOC_004511
7	lnc-KCNN2-2	chr5:113392797-113392871	XLOC_004511
8	lnc-KCNN2-4	chr5:113420696-113420767	l_2997_chr5:113419571-113469367_heart

No data

Variant related genes	Relation type
ENSG00000251628	TF binding region
ENSG00000251628	CpG island

Extended variants
information (count: 4381 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4381 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576555468	chr5:113168652-113168653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527604907	chr5:113168656-113168657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565412428	chr5:113168689-113168690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577431113	chr5:113168702-113168703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541192989	chr5:113168712-113168713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190467061	chr5:113168719-113168720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs137938776	chr5:113168722-113168723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141623632	chr5:113168735-113168736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568154789	chr5:113168830-113168831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535451840	chr5:113168834-113168835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150498341	chr5:113168874-113168875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183383086	chr5:113168901-113168902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377578774	chr5:113168949-113168950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550511969	chr5:113169000-113169001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189835518	chr5:113180400-113180401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79948181	chr5:113180414-113180415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114201039	chr5:113180508-113180509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558903793	chr5:113180528-113180529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574133297	chr5:113180530-113180531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561265465	chr5:113180539-113180540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145247408	chr5:113180555-113180556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1351608	chr5:113180637-113180638	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs1351607	chr5:113180653-113180654	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs530348862	chr5:113180695-113180696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550064809	chr5:113180785-113180786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542096374	chr5:113180827-113180828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374390742	chr5:113180830-113180831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73243066	chr5:113180852-113180853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532851740	chr5:113180869-113180870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs137869152	chr5:113180912-113180913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563332930	chr5:113180917-113180918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566391478	chr5:113180927-113180928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536621344	chr5:113180929-113180930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548607298	chr5:113180966-113180967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570013876	chr5:113180968-113180969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181293216	chr5:113180994-113180995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530418378	chr5:113181017-113181018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13174900	chr5:113181034-113181035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs534591961	chr5:113181060-113181061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184285077	chr5:113181083-113181084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574410706	chr5:113181102-113181103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541375937	chr5:113181206-113181207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563302508	chr5:113181260-113181261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530103190	chr5:113181281-113181282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4299731	chr5:113181289-113181290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs528157326	chr5:113181315-113181316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144659413	chr5:113181320-113181321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111464541	chr5:113181328-113181329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540271646	chr5:113181390-113181391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs900306	chr5:113181396-113181397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113168600-113169000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr5:113180400-113181000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr5:113180600-113181000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr5:113180600-113181000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:113181000-113182400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:113181000-113182400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:113182200-113183600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:113182400-113182600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:113182400-113183800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:113182800-113183200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:113182800-113183600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr5:113182800-113183600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:113182800-113183800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr5:113182800-113183800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:113183000-113183400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:113183000-113183400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:113183400-113183800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:113203200-113203600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:113209600-113210200	Enhancers	Brain Germinal Matrix	brain
20	chr5:113209800-113211000	Enhancers	Fetal Brain Female	brain
21	chr5:113210200-113210600	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr5:113210400-113210800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr5:113210400-113211400	Enhancers	Fetal Brain Male	brain
24	chr5:113210600-113210800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr5:113210600-113213000	Enhancers	Brain Germinal Matrix	brain
26	chr5:113222400-113222600	Enhancers	Aorta	Aorta
27	chr5:113224800-113225200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
28	chr5:113228600-113228800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:113230800-113231000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:113231000-113231200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:113231200-113232600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:113232600-113233000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:113232600-113233800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:113233000-113233800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:113233400-113233800	Enhancers	Fetal Brain Male	brain
36	chr5:113233800-113236400	Weak transcription	Fetal Brain Male	brain
37	chr5:113236400-113236800	Enhancers	Fetal Brain Male	brain
38	chr5:113236600-113236800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:113236600-113236800	Enhancers	Psoas Muscle	Psoas
40	chr5:113236800-113238600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr5:113238000-113238400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:113238000-113239400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:113238600-113239200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:113239200-113239600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:113239400-113239800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:113239600-113239800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr5:113239800-113241000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:113239800-113243000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr5:113241600-113246200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:113245000-113245800	Enhancers	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links