Variant report

Variant	nsv579077
Chromosome Location	chr19:24084419-24490299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3687)
CpG islands
(count:1834)
Chromatin interactive
region (count:127)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3687 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:24183499-24185659	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:24246086-24246527	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:24277965-24278090	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:24324328-24324741	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:24183498-24185658	K562	blood:	n/a	n/a
6	ARID3A	chr19:24269634-24269992	K562	blood:	n/a	n/a
7	ARID3A	chr19:24237256-24237537	HepG2	liver:	n/a	n/a
8	ARID3A	chr19:24216225-24216482	HepG2	liver:	n/a	n/a
9	ARID3A	chr19:24322919-24323218	HepG2	liver:	n/a	n/a
10	ATF1	chr19:24269666-24270047	K562	blood:	n/a	n/a
11	ATF1	chr19:24097373-24097798	K562	blood:	n/a	n/a
12	ATF1	chr19:24246636-24246650	K562	blood:	n/a	n/a
13	ATF1	chr19:24183491-24185180	K562	blood:	n/a	n/a
14	ATF2	chr19:24244964-24245381	GM12878	blood:	n/a	n/a
15	ATF2	chr19:24244936-24245412	GM12878	blood:	n/a	n/a
16	ATF2	chr19:24269632-24269953	GM12878	blood:	n/a	n/a
17	ATF3	chr19:24184039-24184181	K562	blood:	n/a	n/a
18	ATF3	chr19:24183982-24184391	A549	lung:	n/a	n/a
19	ATF3	chr19:24097347-24097690	K562	blood:	n/a	n/a
20	ATF3	chr19:24183418-24183789	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr19:24184009-24184195	K562	blood:	n/a	n/a
22	ATF3	chr19:24184490-24185088	A549	lung:	n/a	n/a
23	ATF3	chr19:24183577-24183767	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr19:24184616-24185158	A549	lung:	n/a	n/a
25	ATF3	chr19:24184025-24184182	HepG2	liver:	n/a	n/a
26	ATF3	chr19:24183370-24183793	A549	lung:	n/a	n/a
27	BACH1	chr19:24390853-24391219	K562	blood:	n/a	n/a
28	BACH1	chr19:24216294-24216452	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr19:24184571-24185665	K562	blood:	n/a	n/a
30	BACH1	chr19:24310904-24310905	K562	blood:	n/a	n/a
31	BACH1	chr19:24270502-24270514	K562	blood:	n/a	n/a
32	BACH1	chr19:24183495-24184312	K562	blood:	n/a	n/a
33	BACH1	chr19:24400119-24400496	K562	blood:	n/a	n/a
34	BATF	chr19:24237294-24237770	GM12878	blood:	n/a	n/a
35	BATF	chr19:24184007-24184218	GM12878	blood:	n/a	n/a
36	BATF	chr19:24237342-24237641	GM12878	blood:	n/a	n/a
37	BATF	chr19:24474206-24474374	GM12878	blood:	n/a	n/a
38	BATF	chr19:24253070-24253438	GM12878	blood:	n/a	chr19:24253275-24253286
39	BATF	chr19:24245028-24245377	GM12878	blood:	n/a	n/a
40	BATF	chr19:24474207-24474368	GM12878	blood:	n/a	n/a
41	BATF	chr19:24184550-24184857	GM12878	blood:	n/a	n/a
42	BCL11A	chr19:24183582-24183758	H1-hESC	embryonic stem cell:	n/a	n/a
43	BCL11A	chr19:24474135-24474384	GM12878	blood:	n/a	n/a
44	BCL11A	chr19:24237418-24237685	GM12878	blood:	n/a	n/a
45	BCL11A	chr19:24474214-24474366	GM12878	blood:	n/a	n/a
46	BCL11A	chr19:24183982-24184247	GM12878	blood:	n/a	n/a
47	BCL11A	chr19:24183530-24183739	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL3	chr19:24183980-24184379	A549	lung:	n/a	n/a
49	BCL3	chr19:24183572-24183744	GM12878	blood:	n/a	n/a
50	BCL3	chr19:24269800-24270463	A549	lung:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:24184550-24184600	BE2_C	brain:	n/a
2	chr19:24182604-24182654	K562	blood:	n/a
3	chr19:24182604-24182654	GM12891	blood:	n/a
4	chr19:24154607-24154657	AG04449	skin:	fetal
5	chr19:24184550-24184600	BE2_C	brain:	n/a
6	chr19:24182604-24182654	K562	blood:	n/a
7	chr19:24182604-24182654	GM12891	blood:	n/a
8	chr19:24154607-24154657	AG04449	skin:	fetal
9	chr19:24345179-24345229	ProgFib	skin:	n/a
10	chr19:24184753-24184803	GM06990	blood:	n/a
11	chr19:24216202-24216252	HAEpiC	amniotic membrane:	n/a
12	chr19:24269968-24270018	AG09319	gingival:	n/a
13	chr19:24155489-24155539	HepG2	liver:	n/a
14	chr19:24269968-24270018	RPTEC	kidney:	n/a
15	chr19:24184762-24184812	HAEpiC	amniotic membrane:	n/a
16	chr19:24182718-24182768	SKMC	muscle:	n/a
17	chr19:24269890-24269940	SK-N-SH	brain:	n/a
18	chr19:24182718-24182768	HAEpiC	amniotic membrane:	n/a
19	chr19:24156884-24156934	HRPEpiC	eye:	n/a
20	chr19:24270007-24270057	HPAEpiC	pulmonary alveolar:	n/a
21	chr19:24154607-24154657	AG09309	skin:	n/a
22	chr19:24182718-24182768	K562	blood:	n/a
23	chr19:24270073-24270123	HUVEC	blood vessel:	n/a
24	chr19:24269975-24270025	NH-A	brain:	n/a
25	chr19:24216269-24216319	MCF10A-Er-Src	breast:	n/a
26	chr19:24184753-24184803	HIPEpiC	eye:	n/a
27	chr19:24184523-24184573	HUVEC	blood vessel:	n/a
28	chr19:24269975-24270025	BE2_C	brain:	n/a
29	chr19:24182837-24182887	SAEC	small airway:	n/a
30	chr19:24182718-24182768	ovcar-3	ovarian:	n/a
31	chr19:24154607-24154657	HepG2	liver:	n/a
32	chr19:24182718-24182768	NT2-D1	testis:	n/a
33	chr19:24184933-24184983	MCF-7	breast:	n/a
34	chr19:24182688-24182738	SK-N-MC	brain:	n/a
35	chr19:24182688-24182738	MCF-7	breast:	n/a
36	chr19:24184660-24184710	SK-N-SH	brain:	n/a
37	chr19:24184523-24184573	A549	lung:	n/a
38	chr19:24184851-24184901	AG10803	skin:	n/a
39	chr19:24184523-24184573	NHBE	bronchial:	n/a
40	chr19:24182688-24182738	AoSMC	blood vessel:	n/a
41	chr19:24184851-24184901	AG09319	gingival:	n/a
42	chr19:24156884-24156934	GM19239	blood:	n/a
43	chr19:24154607-24154657	SK-N-SH_RA	brain:	n/a
44	chr19:24184660-24184710	Caco-2	colon:	n/a
45	chr19:24269890-24269940	LNCaP	prostate:	n/a
46	chr19:24345179-24345229	MCF-7	breast:	n/a
47	chr19:24184550-24184600	HL-60	blood:	n/a
48	chr19:24156884-24156934	K562	blood:	n/a
49	chr19:24184851-24184901	MCF-7	breast:	n/a
50	chr19:24270073-24270123	ECC-1	luminal epithelium:	n/a

(count:127 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:24183698..24186253-chr2:133010463..133012247,3	K562	blood:
2	chr19:24216051..24217841-chr19:24269020..24271219,2	MCF-7	breast:
3	chr17:33477643..33478302-chr19:24184476..24185300,2	K562	blood:
4	chr19:24183609..24184220-chr5:71146242..71147243,4	MCF-7	breast:
5	chr19:24121908..24123986-chr19:24125230..24127009,2	MCF-7	breast:
6	chr16:47538608..47539232-chr19:24184323..24185236,2	MCF-7	breast:
7	chr19:24216611..24218601-chr19:24223296..24225894,2	K562	blood:
8	chr19:24309408..24311273-chr19:24321594..24323328,2	MCF-7	breast:
9	chr19:24183629..24184220-chr2:230045099..230046085,2	MCF-7	breast:
10	chr19:24173529..24175347-chr19:24179956..24182069,2	MCF-7	breast:
11	chr19:24183610..24184220-chr5:71146241..71147357,5	MCF-7	breast:
12	chr19:23456603..23457127-chr19:24215859..24216611,4	MCF-7	breast:
13	chr19:24184114..24184636-chr2:133038429..133039143,2	MCF-7	breast:
14	chr19:24183615..24184637-chr4:70296138..70296644,3	K562	blood:
15	chr19:24098019..24099596-chr19:24100994..24103194,2	K562	blood:
16	chr19:24179938..24183018-chr19:24183132..24186058,3	K562	blood:
17	chr19:24264646..24268309-chr19:24268403..24270705,3	MCF-7	breast:
18	chr16:33963670..33966726-chr19:24184116..24187308,5	K562	blood:
19	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
20	chr11:85195169..85196687-chr19:24184953..24186982,2	MCF-7	breast:
21	chr11:85194707..85195726-chr19:24185012..24186176,4	MCF-7	breast:
22	chr19:24208713..24212092-chr19:24216129..24218537,3	K562	blood:
23	chr19:24215951..24218538-chr19:24221383..24223911,4	MCF-7	breast:
24	chr19:24183126..24185198-chr5:71145386..71148247,2	MCF-7	breast:
25	chr19:24183680..24184220-chr2:230045001..230045516,2	MCF-7	breast:
26	chr19:24181292..24184068-chr19:24184818..24187065,2	MCF-7	breast:
27	chr19:24113206..24114972-chr19:24116698..24118505,2	K562	blood:
28	chr19:24253983..24255588-chr19:24260053..24261773,2	K562	blood:
29	chr19:24214637..24216513-chr19:24268176..24271021,2	K562	blood:
30	chr19:24183267..24184972-chr2:133036687..133040151,3	K562	blood:
31	chr1:91851367..91853065-chr19:24182409..24185198,2	MCF-7	breast:
32	chr19:24190718..24193776-chr19:24211395..24214103,3	K562	blood:
33	chr11:85193664..85196579-chr19:24184471..24186975,3	MCF-7	breast:
34	chr1:121483249..121485033-chr19:24456855..24458356,4	K562	blood:
35	chr19:24214690..24216513-chr19:24269521..24272423,2	K562	blood:
36	chr19:24217068..24219436-chr19:24220648..24223132,2	K562	blood:
37	chr19:24184476..24185016-chr6:133593470..133593971,2	MCF-7	breast:
38	chr19:24269905..24270406-chr19:47616316..47616816,2	Hela-S3	cervix:
39	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
40	chr16:47538731..47540646-chr19:24183961..24186504,3	K562	blood:
41	chr19:24309408..24311273-chr19:24321594..24323328,2	MCF-7	breast:
42	chr19:24098019..24099596-chr19:24100994..24103194,2	K562	blood:
43	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
44	chr19:24215256..24217885-chr19:24218600..24221370,4	MCF-7	breast:
45	chr19:23597107..23600085-chr19:24215651..24217575,2	MCF-7	breast:
46	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
47	chr17:33477647..33478335-chr19:24185255..24186286,3	MCF-7	breast:
48	chr19:24215685..24217205-chr19:24228319..24230733,2	MCF-7	breast:
49	chr19:24097706..24100500-chr19:24267529..24270344,3	K562	blood:
50	chr19:24121908..24123986-chr19:24125230..24127009,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF254-1	chr19:24240733-24240767	NONHSAT063955
2	lnc-ZNF681-4	chr19:24231276-24231697	NONHSAT063954
3	lnc-ZNF726-3	chr19:24286988-24290154	NONHSAT063958
4	lnc-ZNF681-2	chr19:24140533-24140732	ENSG00000104777
5	lnc-ZNF681-4	chr19:24245777-24246420	NONHSAT063954
6	lnc-ZNF681-5	chr19:24281227-24281782	NONHSAT063956
7	lnc-ZNF681-4	chr19:24231737-24231816	NONHSAT063954
8	lnc-ZNF726-2	chr19:24218834-24223805	NONHSAT063953
9	lnc-ZNF681-2	chr19:24140533-24141028	NONHSAT063949
10	lnc-ZNF254-1	chr19:24232253-24232641	NONHSAT063955
11	lnc-ZNF681-2	chr19:24134972-24135238	ENSG00000104777
12	lnc-ZNF681-6	chr19:24344995-24346249	NONHSAT063959
13	lnc-ZNF681-2	chr19:24101883-24103000	ENSG00000104777
14	lnc-ZNF681-4	chr19:24240392-24241030	NONHSAT063954
15	lnc-ZNF681-2	chr19:24134950-24135238	NONHSAT063949
16	lnc-ZNF254-2	chr19:24118022-24118975	NONHSAT063946
17	lnc-ZNF681-4	chr19:24242644-24243263	NONHSAT063954
18	lnc-ZNF681-4	chr19:24232042-24232758	NONHSAT063954
19	lnc-RPSAP58-4	chr19:24110590-24112089	ENSG00000269397.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF254	hsa-miR-155-5p	chr19:24312469-24312491
2	ZNF254	hsa-miR-155-5p	chr19:24311154-24311177

Variant related genes	Relation type
ZNF726	TF binding region
ZNF92P3	TF binding region
HAVCR1P1	TF binding region
ZNF254	TF binding region
RNA5-8SP4	TF binding region
ENSG00000269397	TF binding region
ENSG00000268058	TF binding region
ENSG00000268362	TF binding region
ENSG00000269289	TF binding region
ZNF726	CpG island
ZNF92P3	CpG island
HAVCR1P1	CpG island
ZNF254	CpG island
RNA5-8SP4	CpG island
ENSG00000269397	CpG island
ENSG00000268058	CpG island
ENSG00000268362	CpG island
ENSG00000269289	CpG island
ENSG00000272256	chromatin interactions
ENSG00000269289	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000213971	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000222268	chromatin interactions
ENSG00000268058	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000269416	chromatin interactions
ENSG00000133872	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000202174	chromatin interactions
ENSG00000213967	chromatin interactions
ENSG00000268362	chromatin interactions
ENSG00000183850	chromatin interactions
ENSG00000269421	chromatin interactions
ENSG00000221288	chromatin interactions
RALB	miRNA target sites
PGRMC1	miRNA target sites

Extended variants
information (count: 16923 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:16923 , 50 per page) page: 1 2 3 4 5 6 7 ... 339

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6511674	chr19:24084419-24084420	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557233728	chr19:24084443-24084444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575314271	chr19:24084471-24084472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149251200	chr19:24084487-24084488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79538361	chr19:24084489-24084490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10451493	chr19:24084504-24084505	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs112129164	chr19:24084559-24084560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184938304	chr19:24084561-24084562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542416612	chr19:24084571-24084572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544543690	chr19:24084578-24084579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555897771	chr19:24084599-24084600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74439071	chr19:24084607-24084608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527515843	chr19:24084617-24084618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112043171	chr19:24084635-24084636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530209980	chr19:24084655-24084656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565263469	chr19:24084664-24084665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548831985	chr19:24084682-24084683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143481155	chr19:24084763-24084764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114544493	chr19:24084771-24084772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143557792	chr19:24084772-24084773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189975758	chr19:24084777-24084778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538256359	chr19:24084812-24084813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376588734	chr19:24084850-24084851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147191991	chr19:24084851-24084852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536024492	chr19:24084852-24084853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554384561	chr19:24084867-24084868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35914128	chr19:24084936-24084937	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539894543	chr19:24084950-24084951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374014742	chr19:24084953-24084954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530010166	chr19:24085000-24085001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573896094	chr19:24087804-24087805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs527452357	chr19:24087873-24087874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs541083500	chr19:24087953-24087954	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs375697608	chr19:24087958-24087959	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs193001956	chr19:24088049-24088050	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs577938645	chr19:24088058-24088059	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs545102607	chr19:24088061-24088062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564391865	chr19:24088100-24088101	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs112782879	chr19:24088101-24088102	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs188090342	chr19:24088103-24088104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs115942363	chr19:24088106-24088107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs73530038	chr19:24088113-24088114	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368171527	chr19:24088120-24088121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs115397898	chr19:24088133-24088134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs142431360	chr19:24088146-24088147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs192904349	chr19:24088182-24088183	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs551128911	chr19:24088237-24088238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55751767	chr19:24088260-24088261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs537300436	chr19:24088318-24088319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549273164	chr19:24088359-24088360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:5302 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:24084000-24085000	Enhancers	Colonic Mucosa	Colon
2	chr19:24087800-24088200	ZNF genes & repeats	Liver	Liver
3	chr19:24088200-24089200	Weak transcription	Liver	Liver
4	chr19:24089200-24093000	Enhancers	Liver	Liver
5	chr19:24093000-24094800	Weak transcription	Liver	Liver
6	chr19:24094800-24095000	Enhancers	Liver	Liver
7	chr19:24094800-24097200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr19:24095000-24095200	Weak transcription	Liver	Liver
9	chr19:24095200-24095600	Enhancers	Liver	Liver
10	chr19:24095600-24097200	Weak transcription	Liver	Liver
11	chr19:24095800-24096000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr19:24096000-24096800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr19:24096400-24096600	Enhancers	Dnd41	blood
14	chr19:24096600-24097200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:24096600-24097400	Enhancers	Fetal Brain Male	brain
16	chr19:24096600-24097400	Flanking Active TSS	Dnd41	blood
17	chr19:24096600-24098000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr19:24096600-24098400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr19:24096600-24099200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr19:24096800-24097000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr19:24096800-24097000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr19:24096800-24097000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:24096800-24097000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr19:24096800-24097000	Enhancers	Fetal Muscle Trunk	muscle
25	chr19:24096800-24097000	Enhancers	Placenta	Placenta
26	chr19:24096800-24097200	Enhancers	Primary T cells fromperipheralblood	blood
27	chr19:24096800-24097200	ZNF genes & repeats	K562	blood
28	chr19:24096800-24098000	Active TSS	Primary B cells from cord blood	blood
29	chr19:24096800-24098000	Active TSS	Adipose Nuclei	Adipose
30	chr19:24096800-24098200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:24096800-24098200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr19:24096800-24098400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
33	chr19:24096800-24098400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr19:24096800-24098600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:24096800-24098600	Active TSS	NHDF-Ad	bronchial
36	chr19:24096800-24098800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr19:24097000-24097200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr19:24097000-24097200	Enhancers	Primary B cells from peripheral blood	blood
39	chr19:24097000-24097200	Enhancers	Primary hematopoietic stem cells	blood
40	chr19:24097000-24097200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr19:24097000-24097200	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr19:24097000-24097200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr19:24097000-24097400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr19:24097000-24097400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr19:24097000-24097400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr19:24097000-24097400	Flanking Active TSS	Fetal Muscle Trunk	muscle
47	chr19:24097000-24097400	Flanking Active TSS	Placenta	Placenta
48	chr19:24097000-24097600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr19:24097000-24097800	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr19:24097000-24098000	Active TSS	Primary T regulatory cells fromperipheralblood	blood

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