Variant report

Variant	nsv904548
Chromosome Location	chr15:99940221-99979418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:1286)
Chromatin interactive
region (count:57)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:99949291-99949503	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:99961418-99962008	HepG2	liver:	n/a	n/a
3	ATF2	chr15:99949312-99949582	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr15:99965347-99965754	GM12878	blood:	n/a	n/a
5	BACH1	chr15:99942786-99942799	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:99965364-99965661	GM12878	blood:	n/a	chr15:99965442-99965451
7	BCL3	chr15:99951803-99952015	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:99943953-99944250	K562	blood:	n/a	n/a
9	BHLHE40	chr15:99973687-99973691	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:99961440-99962002	HepG2	liver:	n/a	n/a
11	BHLHE40	chr15:99965453-99965469	K562	blood:	n/a	n/a
12	BRCA1	chr15:99975665-99975680	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr15:99949340-99949473	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr15:99953268-99953329	Hela-S3	cervix:	n/a	chr15:99953308-99953319
15	CEBPB	chr15:99961492-99961572	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:99961370-99961725	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:99953270-99953426	A549	lung:	n/a	chr15:99953308-99953319
18	CEBPB	chr15:99961361-99961734	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:99965381-99965715	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:99961467-99961647	HepG2	liver:	n/a	n/a
21	CEBPB	chr15:99953257-99953373	IMR90	lung:	n/a	chr15:99953308-99953319
22	CEBPB	chr15:99953294-99953334	HepG2	liver:	n/a	chr15:99953308-99953319
23	CEBPB	chr15:99961470-99961726	MCF-7	breast:	n/a	n/a
24	CEBPB	chr15:99965407-99965607	Hela-S3	cervix:	n/a	n/a
25	CEBPD	chr15:99961442-99961604	HepG2	liver:	n/a	n/a
26	CHD2	chr15:99961572-99961672	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:99961599-99961785	HepG2	liver:	n/a	n/a
28	CHD2	chr15:99949310-99949503	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr15:99965573-99965713	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr15:99975690-99975908	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr15:99949434-99949508	HepG2	liver:	n/a	n/a
32	CHD2	chr15:99973694-99973933	GM12878	blood:	n/a	n/a
33	CHD2	chr15:99973825-99973857	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr15:99949239-99949599	A549	lung:	n/a	n/a
35	CTCF	chr15:99949360-99949510	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr15:99966260-99966410	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr15:99966260-99966410	HCT-116	colon:	n/a	n/a
38	CTCF	chr15:99973798-99973839	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr15:99966260-99966410	GM12873	blood:	n/a	n/a
40	CTCF	chr15:99966340-99966490	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr15:99975580-99975730	NHEK	skin:	n/a	n/a
42	CTCF	chr15:99949320-99949470	HMEC	breast:	n/a	n/a
43	CTCF	chr15:99966200-99966350	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr15:99966218-99966397	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr15:99949316-99949498	GM10248	blood:	n/a	n/a
46	CTCF	chr15:99949340-99949490	GM12872	blood:	n/a	n/a
47	CTCF	chr15:99949380-99949530	HCM	heart:	n/a	n/a
48	CTCF	chr15:99949289-99949556	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:99949320-99949470	GM12870	blood:	n/a	n/a
50	CTCF	chr15:99949280-99949577	MCF-7	breast:	n/a	n/a

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99949289-99949339	Hela-S3	cervix:	n/a
2	chr15:99971213-99971263	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:99971213-99971263	PANC-1	pancreas:	n/a
4	chr15:99975470-99975520	HAEpiC	amniotic membrane:	n/a
5	chr15:99966833-99966883	AG04450	lung:	fetal
6	chr15:99949289-99949339	Hela-S3	cervix:	n/a
7	chr15:99971213-99971263	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:99971213-99971263	PANC-1	pancreas:	n/a
9	chr15:99975470-99975520	HAEpiC	amniotic membrane:	n/a
10	chr15:99966833-99966883	AG04450	lung:	fetal
11	chr15:99966968-99967018	GM12878	blood:	n/a
12	chr15:99979013-99979063	HMEC	breast:	n/a
13	chr15:99975141-99975191	HMEC	breast:	n/a
14	chr15:99975141-99975191	MCF10A-Er-Src	breast:	n/a
15	chr15:99966833-99966883	HCT-116	colon:	n/a
16	chr15:99979013-99979063	HepG2	liver:	n/a
17	chr15:99978986-99979036	SAEC	small airway:	n/a
18	chr15:99979059-99979109	GM06990	blood:	n/a
19	chr15:99971423-99971473	SKMC	muscle:	n/a
20	chr15:99966968-99967018	NHDF-neo	bronchial:	n/a
21	chr15:99974332-99974382	HCT-116	colon:	n/a
22	chr15:99979389-99979439	K562	blood:	n/a
23	chr15:99975470-99975520	HCF	heart:	n/a
24	chr15:99975334-99975384	NB4	blood:	n/a
25	chr15:99971423-99971473	BJ	skin:	n/a
26	chr15:99971213-99971263	PrEC	prostate:	n/a
27	chr15:99971329-99971379	AG09319	gingival:	n/a
28	chr15:99979346-99979396	HIPEpiC	eye:	n/a
29	chr15:99975470-99975520	PANC-1	pancreas:	n/a
30	chr15:99971329-99971379	K562	blood:	n/a
31	chr15:99966968-99967018	MCF-7	breast:	n/a
32	chr15:99975334-99975384	CMK	blood:	n/a
33	chr15:99975470-99975520	AG04449	skin:	fetal
34	chr15:99979013-99979063	HL-60	blood:	n/a
35	chr15:99949289-99949339	T-47D	breast:	n/a
36	chr15:99967055-99967105	RPTEC	kidney:	n/a
37	chr15:99975334-99975384	IMR90	lung:	fetal
38	chr15:99974881-99974931	AG09309	skin:	n/a
39	chr15:99979059-99979109	ovcar-3	ovarian:	n/a
40	chr15:99979389-99979439	HIPEpiC	eye:	n/a
41	chr15:99975310-99975360	U87	brain:	n/a
42	chr15:99975141-99975191	GM12891	blood:	n/a
43	chr15:99975010-99975060	CMK	blood:	n/a
44	chr15:99949289-99949339	HIPEpiC	eye:	n/a
45	chr15:99949289-99949339	SK-N-MC	brain:	n/a
46	chr15:99975470-99975520	HCM	heart:	n/a
47	chr15:99967055-99967105	HNPCEpiC	eye:	n/a
48	chr15:99949289-99949339	GM12878	blood:	n/a
49	chr15:99975010-99975060	Caco-2	colon:	n/a
50	chr15:99966833-99966883	HIPEpiC	eye:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
2	chr15:99949082..99949796-chr15:99965826..99966399,2	MCF-7	breast:
3	chr15:99949028..99949626-chr15:100295696..100296496,2	MCF-7	breast:
4	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
5	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
6	chr15:99976307..99978594-chr15:100018036..100019822,2	MCF-7	breast:
7	chr15:99962601..99965549-chr15:100104653..100107115,3	MCF-7	breast:
8	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
9	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
10	chr15:99966031..99966539-chr15:100044729..100045649,2	MCF-7	breast:
11	chr15:99966071..99969014-chr15:100104345..100107384,3	MCF-7	breast:
12	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
13	chr15:99949026..99949881-chr15:100243908..100245125,7	MCF-7	breast:
14	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
15	chr15:99941795..99944009-chr15:99945598..99948491,4	K562	blood:
16	chr15:99939354..99941055-chr15:99942585..99945201,2	K562	blood:
17	chr15:99942024..99944742-chr15:99948131..99949840,2	MCF-7	breast:
18	chr15:99947710..99950479-chr15:99955909..99957738,2	MCF-7	breast:
19	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
20	chr15:99942118..99943929-chr15:100105868..100107742,2	MCF-7	breast:
21	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
22	chr15:99943334..99944866-chr15:99950624..99952403,2	MCF-7	breast:
23	chr15:99943334..99944866-chr15:99950624..99952403,2	MCF-7	breast:
24	chr15:99949149..99950707-chr15:99953216..99956210,2	MCF-7	breast:
25	chr15:99948631..99950805-chr15:100153730..100155690,2	MCF-7	breast:
26	chr15:99948993..99949864-chr15:100244211..100245261,3	MCF-7	breast:
27	chr15:99952846..99955288-chr15:100271943..100274389,2	MCF-7	breast:
28	chr15:99947884..99951610-chr15:100057572..100060447,3	MCF-7	breast:
29	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
30	chr15:99965407..99967484-chr15:99969675..99971240,2	K562	blood:
31	chr15:99965843..99966811-chr15:100243795..100245106,3	MCF-7	breast:
32	chr15:99951575..99954227-chr15:99954620..99956790,2	K562	blood:
33	chr15:99941795..99944009-chr15:99945598..99948491,4	K562	blood:
34	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
35	chr15:99948929..99949922-chr15:100044731..100045793,3	MCF-7	breast:
36	chr15:99947710..99950479-chr15:99955909..99957738,2	MCF-7	breast:
37	chr15:99942972..99945321-chr15:99949749..99952573,2	K562	blood:
38	chr15:99966102..99966691-chr15:100044817..100045390,2	MCF-7	breast:
39	chr15:99976374..99976897-chr15:100105314..100105862,2	Hela-S3	cervix:
40	chr15:99939354..99941055-chr15:99942585..99945201,2	K562	blood:
41	chr15:99964977..99967345-chr15:100103742..100106400,3	MCF-7	breast:
42	chr15:99941795..99944009-chr15:99945598..99948167,3	K562	blood:
43	chr15:99951575..99954227-chr15:99954620..99956790,2	K562	blood:
44	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
45	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
46	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
47	chr15:99949149..99950707-chr15:99953216..99956210,2	MCF-7	breast:
48	chr15:99941795..99944009-chr15:99945598..99948167,3	K562	blood:
49	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
50	chr15:99942024..99944742-chr15:99948131..99949840,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC28-1	chr15:99943447-99943790	XLOC_011382
2	lnc-TTC23-5	chr15:99971261-99971500	l_1247_chr15:99961345-99972053_liver
3	lnc-TTC23-5	chr15:99971676-99972112	l_1247_chr15:99961345-99972053_liver
4	lnc-TTC23-5	chr15:99961346-99963761	l_1247_chr15:99961345-99972053_liver
5	lnc-TTC23-3	chr15:99971033-99971233	ENSG00000259341.1
6	lnc-TTC23-5	chr15:99964546-99965708	l_1247_chr15:99961345-99972053_liver
7	lnc-LRRC28-1	chr15:99946080-99946149	XLOC_011382
8	lnc-TTC23-3	chr15:99967214-99967407	ENSG00000259341.1
9	lnc-LRRC28-1	chr15:99940270-99940339	XLOC_011382
10	lnc-TTC23-2	chr15:99941455-99941520	ENSG00000259760.1

No data

Variant related genes	Relation type
ENSG00000259590	TF binding region
ENSG00000259760	TF binding region
ENSG00000259341	TF binding region
ENSG00000259590	CpG island
ENSG00000259760	CpG island
ENSG00000259341	CpG island
ENSG00000183060	chromatin interactions
ENSG00000259341	chromatin interactions
ENSG00000068305	chromatin interactions

Extended variants
information (count: 1837 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1837 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7181871	chr15:99940221-99940222	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538345770	chr15:99940229-99940230	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143973796	chr15:99940262-99940263	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs566258328	chr15:99940302-99940303	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs190377557	chr15:99940334-99940335	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs374023675	chr15:99940479-99940480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575700029	chr15:99940481-99940482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181329502	chr15:99940515-99940516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112234084	chr15:99940598-99940599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186390676	chr15:99940620-99940621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558790514	chr15:99940623-99940624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577305319	chr15:99940637-99940638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77269220	chr15:99940638-99940639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28432193	chr15:99940716-99940717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374366038	chr15:99940741-99940742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528320913	chr15:99940793-99940794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112484078	chr15:99940823-99940824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540016686	chr15:99940843-99940844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190782464	chr15:99940845-99940846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542526814	chr15:99940849-99940850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182635808	chr15:99940875-99940876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531218250	chr15:99940876-99940877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568014837	chr15:99940885-99940886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377160093	chr15:99940891-99940892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148633480	chr15:99940911-99940912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114782208	chr15:99940914-99940915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532264397	chr15:99940930-99940931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141164093	chr15:99940953-99940954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566295096	chr15:99940976-99940977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564855645	chr15:99941012-99941013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530290743	chr15:99941054-99941055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548900851	chr15:99941130-99941131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570286753	chr15:99941167-99941168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537333177	chr15:99941177-99941178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187951846	chr15:99941228-99941229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570735317	chr15:99941235-99941236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76212703	chr15:99941254-99941255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553014841	chr15:99941295-99941296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116612775	chr15:99941316-99941317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528488457	chr15:99941328-99941329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542375193	chr15:99941346-99941347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150711260	chr15:99941471-99941472	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs139424587	chr15:99941475-99941476	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs543333356	chr15:99941491-99941492	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs386787182	chr15:99941504-99941505	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs531980033	chr15:99941505-99941506	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs112561865	chr15:99941506-99941507	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs559442158	chr15:99941507-99941508	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs75009969	chr15:99941514-99941515	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs386787183	chr15:99941519-99941520	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1069 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99915200-99947400	Weak transcription	Thymus	Thymus
2	chr15:99939200-99940400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr15:99939400-99940400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:99939600-99941600	Weak transcription	Fetal Lung	lung
5	chr15:99939600-99944000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:99940000-99940400	Enhancers	HepG2	liver
7	chr15:99940000-99940600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr15:99940200-99940600	Enhancers	Liver	Liver
9	chr15:99940200-99942600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:99940400-99940600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr15:99940400-99940600	Enhancers	Rectal Smooth Muscle	rectum
12	chr15:99940400-99941600	Weak transcription	HepG2	liver
13	chr15:99940600-99941600	Weak transcription	Liver	Liver
14	chr15:99940600-99948400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:99941200-99942200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:99941400-99943000	Enhancers	Fetal Heart	heart
17	chr15:99941600-99942000	Enhancers	Duodenum Mucosa	Duodenum
18	chr15:99941600-99942400	Weak transcription	Fetal Thymus	thymus
19	chr15:99941600-99942400	Enhancers	HepG2	liver
20	chr15:99941600-99942800	Enhancers	Liver	Liver
21	chr15:99941600-99942800	Enhancers	Stomach Mucosa	stomach
22	chr15:99941600-99943000	Enhancers	Fetal Lung	lung
23	chr15:99941600-99943000	Enhancers	Fetal Stomach	stomach
24	chr15:99941600-99945000	Enhancers	Fetal Muscle Leg	muscle
25	chr15:99941800-99942200	Active TSS	Stomach Smooth Muscle	stomach
26	chr15:99941800-99942600	Enhancers	Small Intestine	intestine
27	chr15:99941800-99942800	Enhancers	HSMMtube	muscle
28	chr15:99941800-99943600	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr15:99941800-99943800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr15:99942000-99942400	Enhancers	Fetal Brain Male	brain
31	chr15:99942000-99942600	Enhancers	NHEK	skin
32	chr15:99942000-99942800	Enhancers	Fetal Kidney	kidney
33	chr15:99942000-99943000	Enhancers	Colon Smooth Muscle	Colon
34	chr15:99942200-99942600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:99942200-99942600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr15:99942200-99942800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr15:99942200-99942800	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr15:99942200-99943200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr15:99942200-99944400	Enhancers	Fetal Muscle Trunk	muscle
40	chr15:99942400-99942600	Enhancers	Brain Germinal Matrix	brain
41	chr15:99942400-99942600	Enhancers	Brain Hippocampus Middle	brain
42	chr15:99942400-99942800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr15:99942400-99942800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr15:99942400-99942800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr15:99942400-99942800	Flanking Active TSS	Fetal Brain Male	brain
46	chr15:99942400-99942800	Enhancers	Fetal Brain Female	brain
47	chr15:99942400-99942800	Enhancers	Right Atrium	heart
48	chr15:99942400-99943000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:99942400-99943000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:99942400-99943000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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