Variant report

Variant	nsv1044733
Chromosome Location	chr15:76120924-76228880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2721)
CpG islands
(count:1954)
Chromatin interactive
region (count:155)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2721 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76191926-76191934	K562	blood:	n/a	n/a
2	ARID3A	chr15:76214100-76214463	K562	blood:	n/a	n/a
3	ARID3A	chr15:76196042-76196346	K562	blood:	n/a	n/a
4	ARID3A	chr15:76195944-76196454	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:76123420-76124202	K562	blood:	n/a	n/a
6	ARID3A	chr15:76194463-76194804	K562	blood:	n/a	n/a
7	ARID3A	chr15:76164767-76165045	K562	blood:	n/a	n/a
8	ARID3A	chr15:76177996-76178411	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:76136649-76136842	K562	blood:	n/a	n/a
10	ARID3A	chr15:76156863-76157147	K562	blood:	n/a	n/a
11	ARID3A	chr15:76222206-76222367	K562	blood:	n/a	n/a
12	ARID3A	chr15:76188108-76188298	K562	blood:	n/a	n/a
13	ARID3A	chr15:76173999-76174023	K562	blood:	n/a	n/a
14	ATF1	chr15:76194517-76194846	K562	blood:	n/a	n/a
15	ATF1	chr15:76208798-76208847	K562	blood:	n/a	n/a
16	ATF1	chr15:76155259-76155429	K562	blood:	n/a	n/a
17	ATF1	chr15:76148791-76148912	K562	blood:	n/a	n/a
18	ATF1	chr15:76123841-76124453	K562	blood:	n/a	n/a
19	ATF1	chr15:76214159-76214601	K562	blood:	n/a	n/a
20	ATF2	chr15:76195953-76196551	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr15:76195969-76196384	GM12878	blood:	n/a	n/a
22	ATF2	chr15:76195877-76196537	GM12878	blood:	n/a	n/a
23	ATF2	chr15:76196623-76197024	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr15:76195939-76196537	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr15:76129165-76129802	GM12878	blood:	n/a	n/a
26	ATF2	chr15:76194562-76195025	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr15:76156853-76157104	K562	blood:	n/a	n/a
28	ATF3	chr15:76195827-76196539	A549	lung:	n/a	n/a
29	ATF3	chr15:76195858-76196891	A549	lung:	n/a	n/a
30	ATF3	chr15:76133013-76133252	K562	blood:	n/a	n/a
31	ATF3	chr15:76132984-76133258	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr15:76132987-76133250	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr15:76195960-76196440	K562	blood:	n/a	n/a
34	BACH1	chr15:76195967-76195969	K562	blood:	n/a	n/a
35	BACH1	chr15:76189389-76189390	K562	blood:	n/a	n/a
36	BACH1	chr15:76139988-76140006	K562	blood:	n/a	n/a
37	BACH1	chr15:76135149-76136412	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr15:76201756-76201909	K562	blood:	n/a	n/a
39	BACH1	chr15:76223369-76223448	K562	blood:	n/a	n/a
40	BATF	chr15:76195996-76196363	GM12878	blood:	n/a	n/a
41	BATF	chr15:76129234-76129593	GM12878	blood:	n/a	chr15:76129410-76129421
42	BCL11A	chr15:76196043-76196321	GM12878	blood:	n/a	chr15:76196222-76196235 chr15:76196193-76196202
43	BCL11A	chr15:76195942-76196464	GM12878	blood:	n/a	chr15:76196222-76196235 chr15:76196193-76196202
44	BCL3	chr15:76135787-76136602	A549	lung:	n/a	n/a
45	BCL3	chr15:76195519-76197135	A549	lung:	n/a	chr15:76196222-76196235 chr15:76196193-76196202 chr15:76196750-76196763
46	BCL3	chr15:76195935-76196542	GM12878	blood:	n/a	chr15:76196222-76196235 chr15:76196193-76196202
47	BCL3	chr15:76195563-76197031	A549	lung:	n/a	chr15:76196222-76196235 chr15:76196193-76196202 chr15:76196750-76196763
48	BCL3	chr15:76134802-76135669	A549	lung:	n/a	n/a
49	BCLAF1	chr15:76195860-76196475	K562	blood:	n/a	chr15:76196222-76196235 chr15:76196193-76196202
50	BCLAF1	chr15:76196637-76197084	GM12878	blood:	n/a	chr15:76196750-76196763

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76225330-76225380	SK-N-SH_RA	brain:	n/a
2	chr15:76196418-76196468	AG09309	skin:	n/a
3	chr15:76225330-76225380	SK-N-SH_RA	brain:	n/a
4	chr15:76196418-76196468	AG09309	skin:	n/a
5	chr15:76159937-76159987	AG04450	lung:	fetal
6	chr15:76197455-76197505	HL-60	blood:	n/a
7	chr15:76135284-76135334	CMK	blood:	n/a
8	chr15:76196055-76196105	AG04450	lung:	fetal
9	chr15:76218542-76218592	HRPEpiC	eye:	n/a
10	chr15:76214616-76214666	K562	blood:	n/a
11	chr15:76196328-76196378	HEK293	kidney:	embryo
12	chr15:76225330-76225380	HRE	kidney:	n/a
13	chr15:76197455-76197505	HIPEpiC	eye:	n/a
14	chr15:76195876-76195926	SK-N-MC	brain:	n/a
15	chr15:76196418-76196468	GM06990	blood:	n/a
16	chr15:76226687-76226737	AG04450	lung:	fetal
17	chr15:76197455-76197505	HCT-116	colon:	n/a
18	chr15:76196150-76196200	LNCaP	prostate:	n/a
19	chr15:76196150-76196200	AG09309	skin:	n/a
20	chr15:76200166-76200216	GM19239	blood:	n/a
21	chr15:76196150-76196200	PANC-1	pancreas:	n/a
22	chr15:76136846-76136896	SKMC	muscle:	n/a
23	chr15:76195522-76195572	BE2_C	brain:	n/a
24	chr15:76136846-76136896	GM19239	blood:	n/a
25	chr15:76225330-76225380	SK-N-MC	brain:	n/a
26	chr15:76135312-76135362	HRCEpiC	kidney:	n/a
27	chr15:76222477-76222527	HAEpiC	amniotic membrane:	n/a
28	chr15:76225330-76225380	SK-N-SH	brain:	n/a
29	chr15:76131635-76131685	SK-N-SH	brain:	n/a
30	chr15:76218542-76218592	PFSK-1	brain:	n/a
31	chr15:76197455-76197505	AoSMC	blood vessel:	n/a
32	chr15:76214616-76214666	NT2-D1	testis:	n/a
33	chr15:76196679-76196729	HNPCEpiC	eye:	n/a
34	chr15:76159937-76159987	MCF10A-Er-Src	breast:	n/a
35	chr15:76135159-76135209	HCM	heart:	n/a
36	chr15:76135312-76135362	HUVEC	blood vessel:	n/a
37	chr15:76164542-76164592	HIPEpiC	eye:	n/a
38	chr15:76196679-76196729	AG04450	lung:	fetal
39	chr15:76222477-76222527	HEEpiC	esophagus:	n/a
40	chr15:76159937-76159987	HEEpiC	esophagus:	n/a
41	chr15:76137847-76137897	IMR90	lung:	fetal
42	chr15:76196055-76196105	SKMC	muscle:	n/a
43	chr15:76226687-76226737	GM06990	blood:	n/a
44	chr15:76222477-76222527	HCPEpiC	choroid plexus:	n/a
45	chr15:76196679-76196729	HUVEC	blood vessel:	n/a
46	chr15:76195876-76195926	GM12878	blood:	n/a
47	chr15:76136875-76136925	K562	blood:	n/a
48	chr15:76196799-76196849	HUVEC	blood vessel:	n/a
49	chr15:76136386-76136436	HRE	kidney:	n/a
50	chr15:76136875-76136925	GM12878	blood:	n/a

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr15:76172673..76175756-chr15:76183628..76185667,3	K562	blood:
2	chr15:76133681..76139746-chr15:76193985..76199740,23	MCF-7	breast:
3	chr15:76134245..76136824-chr15:76150305..76152111,2	MCF-7	breast:
4	chr15:76102059..76103151-chr15:76213899..76214766,4	MCF-7	breast:
5	chr15:76177375..76179318-chr15:76182768..76185723,2	MCF-7	breast:
6	chr15:76134186..76138083-chr15:76192925..76200499,13	K562	blood:
7	chr15:76218432..76221221-chr15:76222501..76224322,2	K562	blood:
8	chr15:76133451..76137775-chr15:76156108..76161375,6	MCF-7	breast:
9	chr15:76135389..76135908-chr5:176853550..176854343,2	Hela-S3	cervix:
10	chr15:76136467..76138938-chr15:76146625..76148978,2	MCF-7	breast:
11	chr15:76125343..76127672-chr15:76128445..76130969,2	MCF-7	breast:
12	chr15:76120011..76122209-chr15:76134014..76135562,2	MCF-7	breast:
13	chr15:76161758..76164592-chr15:76173803..76175503,2	K562	blood:
14	chr15:76120011..76122209-chr15:76134014..76135562,2	MCF-7	breast:
15	chr15:76137201..76139115-chr15:76170470..76172779,2	K562	blood:
16	chr15:52310337..52312699-chr15:76160460..76162429,2	MCF-7	breast:
17	chr15:76195569..76197871-chr15:76204617..76208764,4	K562	blood:
18	chr15:76133453..76135446-chr15:76194231..76197164,2	MCF-7	breast:
19	chr15:76118274..76121230-chr15:76121538..76124527,4	K562	blood:
20	chr15:76119670..76121510-chr15:76125025..76126649,2	MCF-7	breast:
21	chr15:76135872..76137923-chr15:76143662..76145313,3	MCF-7	breast:
22	chr15:76135011..76136849-chr15:76154600..76156725,2	K562	blood:
23	chr15:76133553..76135071-chr15:76150512..76152325,2	MCF-7	breast:
24	chr15:38544112..38545065-chr15:76195734..76196719,2	Hela-S3	cervix:
25	chr15:76136320..76138116-chr15:76204520..76207096,2	MCF-7	breast:
26	chr15:76135173..76137779-chr15:76157818..76161014,3	K562	blood:
27	chr15:76197909..76200277-chr15:76201455..76203414,2	MCF-7	breast:
28	chr15:76107299..76109234-chr15:76120119..76122431,2	MCF-7	breast:
29	chr15:76136933..76140770-chr15:76154598..76157335,3	K562	blood:
30	chr15:76190676..76192900-chr15:76194789..76197660,2	K562	blood:
31	chr15:76119288..76121782-chr15:76196929..76199801,2	MCF-7	breast:
32	chr15:75917263..75918956-chr15:76135075..76137725,2	K562	blood:
33	chr15:76102027..76103101-chr15:76220766..76221842,9	MCF-7	breast:
34	chr15:76157186..76158925-chr15:76160347..76162015,2	MCF-7	breast:
35	chr15:76172673..76175756-chr15:76183628..76185667,3	K562	blood:
36	chr15:76211169..76212903-chr15:76216124..76218574,2	K562	blood:
37	chr15:76135754..76137278-chr15:76196181..76197882,2	K562	blood:
38	chr15:76161758..76164592-chr15:76173803..76175503,2	K562	blood:
39	chr15:76198080..76200117-chr15:76302997..76305301,2	K562	blood:
40	chr15:76173887..76175756-chr15:76183628..76185544,2	K562	blood:
41	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:
42	chr15:76146991..76149009-chr15:76171055..76173285,2	MCF-7	breast:
43	chr13:28194510..28195037-chr15:76196289..76196837,2	Hela-S3	cervix:
44	chr15:75660482..75662699-chr15:76134018..76135657,2	MCF-7	breast:
45	chr15:76190464..76192251-chr15:76192564..76194380,2	K562	blood:
46	chr15:76179685..76181538-chr15:76200237..76202606,2	K562	blood:
47	chr15:76196239..76198362-chr15:76207161..76208693,2	MCF-7	breast:
48	chr15:76195569..76197871-chr15:76205442..76207733,2	K562	blood:
49	chr15:76220909..76222483-chr15:76431367..76432547,6	MCF-7	breast:
50	chr15:76135754..76137278-chr15:76196181..76197882,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRG4-1	chr15:76228310-76228651	NONHSAT047388
2	lnc-NRG4-1	chr15:76228310-76228651	NONHSAT047387
3	lnc-FBXO22-2	chr15:76187381-76187639	NONHSAT047385

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FBXO22	hsa-miR-1	chr15:76222492-76222513
2	FBXO22	hsa-miR-1	chr15:76225787-76225793
3	UBE2Q2	hsa-miR-32-5p	chr15:76192578-76192601
4	FBXO22	hsa-miR-1	chr15:76225772-76225794

Variant related genes	Relation type
RN7SL510P	TF binding region
FBXO22	TF binding region
UBE2Q2	TF binding region
RN7SL510P	CpG island
FBXO22	CpG island
UBE2Q2	CpG island
ENSG00000259438	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000252372	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000166068	chromatin interactions
ENSG00000139517	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000140506	chromatin interactions
ENSG00000140400	chromatin interactions
ENSG00000135845	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000186184	chromatin interactions
ENSG00000111581	chromatin interactions
ENSG00000266308	chromatin interactions
ENSG00000247363	chromatin interactions
ENSG00000187812	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000169371	chromatin interactions

Extended variants
information (count: 3798 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3798 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16967527	chr15:76120924-76120925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527893345	chr15:76120925-76120926	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs142287432	chr15:76120938-76120939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549680867	chr15:76120943-76120944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567987607	chr15:76120957-76120958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537837114	chr15:76120959-76120960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545721041	chr15:76121007-76121008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192199150	chr15:76121135-76121136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184520810	chr15:76121136-76121137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146181361	chr15:76121182-76121183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs137896883	chr15:76121217-76121218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572172509	chr15:76121253-76121254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs74317038	chr15:76121272-76121273	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199883843	chr15:76121291-76121292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375391433	chr15:76121306-76121307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554425007	chr15:76121316-76121317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575978834	chr15:76121361-76121362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559498050	chr15:76121371-76121372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543319545	chr15:76121372-76121373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562492977	chr15:76121398-76121399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571486055	chr15:76121422-76121423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78254307	chr15:76121457-76121458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77988044	chr15:76121530-76121531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541708208	chr15:76121545-76121546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139529517	chr15:76121566-76121567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549639721	chr15:76121601-76121602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35033154	chr15:76121609-76121610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567957087	chr15:76121771-76121772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531995844	chr15:76121800-76121801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149707604	chr15:76121878-76121879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546312377	chr15:76121898-76121899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111749681	chr15:76121899-76121900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571187101	chr15:76121941-76121942	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371333017	chr15:76121954-76121955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190205725	chr15:76121956-76121957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182034221	chr15:76121957-76121958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565669791	chr15:76121964-76121965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs58619115	chr15:76122078-76122079	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs530395242	chr15:76122089-76122090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184303454	chr15:76122118-76122119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368641915	chr15:76122144-76122145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376238311	chr15:76122183-76122184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189072890	chr15:76122186-76122187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577950465	chr15:76122204-76122205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552044218	chr15:76122206-76122207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368878228	chr15:76122215-76122216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560626733	chr15:76122249-76122250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11630657	chr15:76122252-76122253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11630659	chr15:76122264-76122265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181110010	chr15:76122301-76122302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Intellectual disability	22102821	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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:4422 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76116800-76123200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:76116800-76123400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr15:76117000-76122800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr15:76117000-76123200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:76117000-76123800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:76117200-76123000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr15:76118800-76121600	Enhancers	K562	blood
8	chr15:76119400-76121400	Enhancers	NHEK	skin
9	chr15:76119600-76121200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:76119600-76121400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr15:76119600-76121400	Enhancers	HMEC	breast
12	chr15:76119600-76123400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr15:76120000-76123200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:76120200-76123400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr15:76120200-76123400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr15:76120400-76123000	Weak transcription	HSMMtube	muscle
17	chr15:76120400-76123200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr15:76120400-76123200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:76120400-76123200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:76120400-76123400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr15:76120400-76123600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr15:76120600-76123200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:76120800-76124200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:76121200-76128000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:76121400-76123600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:76121400-76124000	Weak transcription	HMEC	breast
27	chr15:76121400-76124400	Weak transcription	NHEK	skin
28	chr15:76121600-76122800	Weak transcription	K562	blood
29	chr15:76122800-76123000	Enhancers	K562	blood
30	chr15:76122800-76125200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr15:76123000-76124600	Enhancers	HSMMtube	muscle
32	chr15:76123000-76124800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr15:76123000-76124800	Flanking Active TSS	K562	blood
34	chr15:76123200-76123400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr15:76123200-76124000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:76123200-76124000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:76123200-76124600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr15:76123200-76124600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:76123200-76124800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr15:76123200-76124800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr15:76123200-76125000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr15:76123400-76123800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr15:76123400-76124000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr15:76123400-76124000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr15:76123400-76124400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr15:76123400-76124400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr15:76123400-76124600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr15:76123400-76124800	Enhancers	H1 Cell Line	embryonic stem cell
49	chr15:76123400-76124800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr15:76123400-76124800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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