Variant report

Variant	nsv540179
Chromosome Location	chr9:100292680-100415269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2311)
CpG islands
(count:795)
Chromatin interactive
region (count:189)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2311 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:100377812-100378112	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:100399332-100399526	K562	blood:	n/a	n/a
3	ARID3A	chr9:100394896-100395762	K562	blood:	n/a	n/a
4	ARID3A	chr9:100394155-100394365	K562	blood:	n/a	n/a
5	ARID3A	chr9:100377792-100378097	K562	blood:	n/a	n/a
6	ARID3A	chr9:100394817-100396132	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:100361010-100361210	K562	blood:	n/a	n/a
8	ATF1	chr9:100302596-100303026	K562	blood:	n/a	n/a
9	ATF1	chr9:100330092-100330410	K562	blood:	n/a	n/a
10	ATF1	chr9:100394928-100396154	K562	blood:	n/a	n/a
11	ATF2	chr9:100394754-100396296	GM12878	blood:	n/a	chr9:100395645-100395656
12	ATF2	chr9:100394768-100396258	GM12878	blood:	n/a	chr9:100395645-100395656
13	ATF2	chr9:100380127-100380754	GM12878	blood:	n/a	n/a
14	ATF2	chr9:100394599-100396120	H1-hESC	embryonic stem cell:	n/a	chr9:100395645-100395656
15	ATF2	chr9:100321121-100321901	GM12878	blood:	n/a	n/a
16	ATF2	chr9:100360714-100361293	GM12878	blood:	n/a	n/a
17	ATF2	chr9:100394654-100395770	H1-hESC	embryonic stem cell:	n/a	chr9:100395645-100395656
18	ATF2	chr9:100321028-100321868	GM12878	blood:	n/a	n/a
19	ATF3	chr9:100395249-100395735	K562	blood:	n/a	chr9:100395647-100395655 chr9:100395647-100395658 chr9:100395645-100395656 chr9:100395647-100395654 chr9:100395646-100395654 chr9:100395643-100395658 chr9:100395645-100395656 chr9:100395647-100395657 chr9:100395643-100395656
20	ATF3	chr9:100305732-100306275	HCT-116	colon:	n/a	n/a
21	ATF3	chr9:100394825-100396088	K562	blood:	n/a	chr9:100395647-100395655 chr9:100395647-100395658 chr9:100395645-100395656 chr9:100395647-100395654 chr9:100395646-100395654 chr9:100395643-100395658 chr9:100395645-100395656 chr9:100395647-100395657 chr9:100395643-100395656
22	ATF3	chr9:100305822-100306352	HCT-116	colon:	n/a	n/a
23	BACH1	chr9:100404533-100404695	K562	blood:	n/a	n/a
24	BACH1	chr9:100395717-100396308	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr9:100380116-100380658	GM12878	blood:	n/a	chr9:100380523-100380531
26	BATF	chr9:100321390-100321775	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:100321429-100321849	GM12878	blood:	n/a	n/a
28	BCL3	chr9:100364317-100364773	K562	blood:	n/a	n/a
29	BCL3	chr9:100321354-100321844	GM12878	blood:	n/a	n/a
30	BCL3	chr9:100395169-100396180	A549	lung:	n/a	chr9:100395612-100395621
31	BCL3	chr9:100394858-100396305	A549	lung:	n/a	chr9:100395612-100395621
32	BCL3	chr9:100395379-100396278	GM12878	blood:	n/a	chr9:100395612-100395621
33	BCLAF1	chr9:100394963-100396297	GM12878	blood:	n/a	chr9:100395612-100395621
34	BCLAF1	chr9:100395266-100396192	K562	blood:	n/a	chr9:100395612-100395621
35	BCLAF1	chr9:100321013-100321917	GM12878	blood:	n/a	n/a
36	BCLAF1	chr9:100360812-100361390	GM12878	blood:	n/a	n/a
37	BCLAF1	chr9:100394771-100396057	K562	blood:	n/a	chr9:100395612-100395621
38	BCLAF1	chr9:100395021-100396733	GM12878	blood:	n/a	chr9:100396673-100396682 chr9:100395612-100395621 chr9:100396377-100396386 chr9:100396312-100396321
39	BHLHE40	chr9:100360914-100361294	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:100395193-100395588	HepG2	liver:	n/a	chr9:100395405-100395414 chr9:100395405-100395414
41	BHLHE40	chr9:100394615-100396533	GM12878	blood:	n/a	chr9:100395405-100395414 chr9:100395405-100395414
42	BHLHE40	chr9:100326615-100326730	A549	lung:	n/a	n/a
43	BHLHE40	chr9:100394879-100396319	HepG2	liver:	n/a	chr9:100395405-100395414 chr9:100395405-100395414
44	BHLHE40	chr9:100395022-100395945	A549	lung:	n/a	chr9:100395405-100395414 chr9:100395405-100395414
45	BHLHE40	chr9:100395186-100395608	HepG2	liver:	n/a	chr9:100395405-100395414 chr9:100395405-100395414
46	BHLHE40	chr9:100361131-100361411	K562	blood:	n/a	n/a
47	BHLHE40	chr9:100377911-100378009	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:100326577-100326858	K562	blood:	n/a	n/a
49	BHLHE40	chr9:100326691-100326885	HepG2	liver:	n/a	n/a
50	BHLHE40	chr9:100330053-100330500	K562	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:100394654-100394704	PrEC	prostate:	n/a
2	chr9:100394496-100394546	MCF-7	breast:	n/a
3	chr9:100394654-100394704	PrEC	prostate:	n/a
4	chr9:100394496-100394546	MCF-7	breast:	n/a
5	chr9:100389634-100389684	SK-N-SH_RA	brain:	n/a
6	chr9:100396777-100396827	NHBE	bronchial:	n/a
7	chr9:100396413-100396463	SAEC	small airway:	n/a
8	chr9:100398470-100398520	IMR90	lung:	fetal
9	chr9:100395349-100395399	HRE	kidney:	n/a
10	chr9:100396413-100396463	T-47D	breast:	n/a
11	chr9:100398470-100398520	K562	blood:	n/a
12	chr9:100394654-100394704	MCF10A-Er-Src	breast:	n/a
13	chr9:100398470-100398520	ProgFib	skin:	n/a
14	chr9:100394496-100394546	HCT-116	colon:	n/a
15	chr9:100396413-100396463	CMK	blood:	n/a
16	chr9:100396413-100396463	HUVEC	blood vessel:	n/a
17	chr9:100396302-100396352	BJ	skin:	n/a
18	chr9:100396098-100396148	HRPEpiC	eye:	n/a
19	chr9:100398470-100398520	PrEC	prostate:	n/a
20	chr9:100394654-100394704	HEK293	kidney:	embryo
21	chr9:100326029-100326079	CMK	blood:	n/a
22	chr9:100398470-100398520	AG09309	skin:	n/a
23	chr9:100389634-100389684	MCF10A-Er-Src	breast:	n/a
24	chr9:100326029-100326079	HMEC	breast:	n/a
25	chr9:100396098-100396148	BJ	skin:	n/a
26	chr9:100395413-100395463	HMEC	breast:	n/a
27	chr9:100396477-100396527	NT2-D1	testis:	n/a
28	chr9:100395413-100395463	PANC-1	pancreas:	n/a
29	chr9:100398470-100398520	HNPCEpiC	eye:	n/a
30	chr9:100394496-100394546	H1-hESC	embryonic stem cell:	embryo
31	chr9:100395349-100395399	AG10803	skin:	n/a
32	chr9:100326029-100326079	LNCaP	prostate:	n/a
33	chr9:100396477-100396527	SK-N-SH_RA	brain:	n/a
34	chr9:100389634-100389684	GM06990	blood:	n/a
35	chr9:100396477-100396527	SKMC	muscle:	n/a
36	chr9:100396098-100396148	HEK293	kidney:	embryo
37	chr9:100396777-100396827	AG09319	gingival:	n/a
38	chr9:100396413-100396463	SK-N-SH_RA	brain:	n/a
39	chr9:100398470-100398520	U87	brain:	n/a
40	chr9:100396477-100396527	U87	brain:	n/a
41	chr9:100396302-100396352	ovcar-3	ovarian:	n/a
42	chr9:100326029-100326079	HRPEpiC	eye:	n/a
43	chr9:100394496-100394546	A549	lung:	n/a
44	chr9:100326029-100326079	Jurkat	blood:	n/a
45	chr9:100395349-100395399	HEEpiC	esophagus:	n/a
46	chr9:100396302-100396352	GM12878	blood:	n/a
47	chr9:100396477-100396527	HPAEpiC	pulmonary alveolar:	n/a
48	chr9:100394496-100394546	HUVEC	blood vessel:	n/a
49	chr9:100326029-100326079	SAEC	small airway:	n/a
50	chr9:100395349-100395399	Hepatocyte	liver:	n/a

(count:189 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:100264233..100266882-chr9:100385504..100387245,2	MCF-7	breast:
2	chr9:100377595..100379440-chr9:100388100..100390147,2	K562	blood:
3	chr9:100359880..100362993-chr9:100364849..100367114,3	K562	blood:
4	chr9:100413361..100415528-chr9:100417013..100418852,2	K562	blood:
5	chr9:100358063..100359850-chr9:100366510..100368844,2	MCF-7	breast:
6	chr9:100371781..100375300-chr9:100375938..100379259,4	K562	blood:
7	chr9:100393858..100397326-chr9:100457081..100460285,5	MCF-7	breast:
8	chr9:100296309..100298470-chr9:100299866..100302323,2	K562	blood:
9	chr9:100411427..100413125-chr9:100414736..100416807,2	K562	blood:
10	chr9:100289928..100292573-chr9:100328565..100332517,3	K562	blood:
11	chr9:100403992..100406987-chr9:100418866..100421676,2	K562	blood:
12	chr9:100148879..100149573-chr9:100377949..100378512,2	MCF-7	breast:
13	chr9:100228650..100231026-chr9:100395241..100396818,2	K562	blood:
14	chr9:100319150..100321068-chr9:100324699..100328167,3	K562	blood:
15	chr9:100174026..100174653-chr9:100360559..100361581,3	K562	blood:
16	chr9:100365045..100368073-chr9:100391835..100395201,3	K562	blood:
17	chr9:100292941..100294697-chr9:100298496..100300726,2	K562	blood:
18	chr9:100310351..100312765-chr9:100313223..100315072,2	K562	blood:
19	chr9:100371781..100375300-chr9:100375938..100379259,4	K562	blood:
20	chr17:80374866..80376675-chr9:100395383..100397394,2	MCF-7	breast:
21	chr9:100399929..100403095-chr9:100406976..100411224,3	MCF-7	breast:
22	chr1:28974912..28975848-chr9:100395311..100396221,2	Hela-S3	cervix:
23	chr9:100355062..100357246-chr9:100361025..100362574,2	MCF-7	breast:
24	chr9:100393929..100396893-chr9:100683273..100687162,3	K562	blood:
25	chr9:100318639..100320970-chr9:100327548..100329985,2	MCF-7	breast:
26	chr9:100377919..100379594-chr9:100390276..100392003,2	MCF-7	breast:
27	chr9:100408553..100411493-chr9:100458323..100460907,2	MCF-7	breast:
28	chr9:100331492..100333368-chr9:100335840..100338156,2	K562	blood:
29	chr9:100361363..100362991-chr9:100365453..100368100,2	MCF-7	breast:
30	chr9:100172589..100175955-chr9:100393372..100395869,4	K562	blood:
31	chr9:100263609..100264267-chr9:100360719..100361387,4	MCF-7	breast:
32	chr9:100173782..100174687-chr9:100361010..100361547,3	MCF-7	breast:
33	chr9:100230612..100231556-chr9:100377483..100378918,12	MCF-7	breast:
34	chr9:100404481..100406346-chr9:100406637..100409323,4	MCF-7	breast:
35	chr9:100410166..100412202-chr9:100420931..100422531,3	K562	blood:
36	chr9:100158859..100160754-chr9:100392262..100394128,2	K562	blood:
37	chr9:100307811..100310767-chr9:100315037..100317582,2	MCF-7	breast:
38	chr9:100148966..100149836-chr9:100377517..100378454,2	K562	blood:
39	chr16:3332578..3333236-chr9:100395488..100396139,2	HCT-116	colon:
40	chr9:100365847..100368538-chr9:100369837..100371571,2	K562	blood:
41	chr9:100405436..100408239-chr9:100423009..100425764,2	K562	blood:
42	chr9:100284003..100288374-chr9:100289248..100292769,6	K562	blood:
43	chr12:132194912..132195812-chr9:100366402..100367362,2	NB4	blood:
44	chr9:100403670..100406191-chr9:100444753..100446885,2	MCF-7	breast:
45	chr9:100279156..100280709-chr9:100395787..100397430,2	K562	blood:
46	chr9:100371893..100374516-chr9:100380257..100382614,2	MCF-7	breast:
47	chr9:100313497..100316330-chr9:100393433..100395360,2	MCF-7	breast:
48	chr9:100410035..100412415-chr9:100683704..100685557,2	MCF-7	breast:
49	chr9:100295100..100296827-chr9:100298113..100299866,2	K562	blood:
50	chr9:100311264..100313997-chr9:100315721..100318080,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSTD2-1	chr9:100398070-100398148	ENSG00000231521.1
2	lnc-TSTD2-1	chr9:100396797-100396913	ENSG00000231521.1
3	lnc-TSTD2-1	chr9:100398245-100398333	ENSG00000231521.1

No data

Variant related genes	Relation type
ENSG00000231521	TF binding region
NCBP1	TF binding region
TSTD2	TF binding region
TMOD1	TF binding region
ENSG00000231521	CpG island
NCBP1	CpG island
TSTD2	CpG island
TMOD1	CpG island
ENSG00000136938	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000181396	chromatin interactions
ENSG00000201239	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000178449	chromatin interactions
ENSG00000272368	chromatin interactions
ENSG00000108854	chromatin interactions
ENSG00000169660	chromatin interactions
ENSG00000136936	chromatin interactions
ENSG00000006194	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000196116	chromatin interactions
ENSG00000136925	chromatin interactions
ENSG00000063177	chromatin interactions
ENSG00000136937	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000073578	chromatin interactions
ENSG00000061936	chromatin interactions
ENSG00000136842	chromatin interactions
ENSG00000201830	chromatin interactions
ENSG00000106780	chromatin interactions
ENSG00000261135	chromatin interactions
ENSG00000148337	chromatin interactions
ENSG00000197816	chromatin interactions
ENSG00000228174	chromatin interactions

Extended variants
information (count: 4471 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4471 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542489228	chr9:100292728-100292729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563876283	chr9:100292751-100292752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530987237	chr9:100292752-100292753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552721656	chr9:100292753-100292754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368303909	chr9:100292808-100292809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376110835	chr9:100292809-100292810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201236779	chr9:100292863-100292864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564298057	chr9:100292869-100292870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553984736	chr9:100292877-100292878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528518354	chr9:100292882-100292883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372287884	chr9:100292915-100292916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180685265	chr9:100292919-100292920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545813327	chr9:100292929-100292930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372731724	chr9:100292933-100292934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568725072	chr9:100292979-100292980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539117645	chr9:100292988-100292989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58309253	chr9:100293051-100293052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11434863	chr9:100293070-100293071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57086657	chr9:100293088-100293089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572734660	chr9:100293093-100293094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533825582	chr9:100293105-100293106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553387850	chr9:100293118-100293119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575139699	chr9:100293131-100293132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542550231	chr9:100293138-100293139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563839031	chr9:100293156-100293157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572790400	chr9:100293193-100293194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575932977	chr9:100293194-100293195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546300615	chr9:100293203-100293204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564640358	chr9:100293284-100293285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202030181	chr9:100293315-100293316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528469584	chr9:100293316-100293317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374714014	chr9:100293319-100293320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557982424	chr9:100293321-100293322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563049811	chr9:100293323-100293324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561944752	chr9:100293324-100293325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564046583	chr9:100293325-100293326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529116457	chr9:100293326-100293327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550481428	chr9:100293424-100293425	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568688296	chr9:100293435-100293436	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190178377	chr9:100293442-100293443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551178491	chr9:100293488-100293489	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377141925	chr9:100293543-100293544	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140550529	chr9:100293551-100293552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566609375	chr9:100293724-100293725	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533653329	chr9:100293731-100293732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539269608	chr9:100293754-100293755	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150443759	chr9:100293764-100293765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536129469	chr9:100293775-100293776	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183380457	chr9:100293782-100293783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566513981	chr9:100293786-100293787	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3889 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100274000-100318400	Weak transcription	Gastric	stomach
2	chr9:100284600-100318400	Weak transcription	Liver	Liver
3	chr9:100289600-100292800	Enhancers	Colon Smooth Muscle	Colon
4	chr9:100289600-100295000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr9:100290400-100294400	Weak transcription	Fetal Brain Male	brain
6	chr9:100290600-100295600	Weak transcription	Fetal Brain Female	brain
7	chr9:100290600-100296800	Weak transcription	Pancreas	Pancrea
8	chr9:100291200-100296200	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:100291400-100294200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr9:100291600-100293400	Weak transcription	K562	blood
11	chr9:100291600-100294000	Enhancers	Fetal Heart	heart
12	chr9:100291600-100294200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:100291600-100294200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:100291600-100294400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr9:100291600-100297600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:100291600-100317200	Weak transcription	Brain Angular Gyrus	brain
17	chr9:100291800-100294000	Weak transcription	Fetal Stomach	stomach
18	chr9:100291800-100296600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr9:100292200-100293400	Weak transcription	Ovary	ovary
20	chr9:100292200-100293800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:100292200-100293800	Weak transcription	Brain Anterior Caudate	brain
22	chr9:100292200-100294200	Weak transcription	NHLF	lung
23	chr9:100292200-100295000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr9:100292200-100309400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr9:100292200-100310600	Weak transcription	Lung	lung
26	chr9:100292400-100293400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr9:100292400-100293600	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:100292400-100293800	Weak transcription	Left Ventricle	heart
29	chr9:100292400-100293800	Weak transcription	Psoas Muscle	Psoas
30	chr9:100292400-100293800	Weak transcription	Right Atrium	heart
31	chr9:100292400-100293800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:100292400-100293800	Weak transcription	HSMMtube	muscle
33	chr9:100292400-100294000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:100292400-100294000	Weak transcription	Aorta	Aorta
35	chr9:100292400-100294000	Weak transcription	Right Ventricle	heart
36	chr9:100292400-100296200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:100292600-100293600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr9:100292600-100293800	Weak transcription	GM12878-XiMat	blood
39	chr9:100292800-100293800	Weak transcription	Colon Smooth Muscle	Colon
40	chr9:100293400-100293800	Enhancers	Ovary	ovary
41	chr9:100293400-100294000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr9:100293400-100301600	Strong transcription	K562	blood
43	chr9:100293600-100294800	Enhancers	Fetal Muscle Leg	muscle
44	chr9:100293600-100295400	Enhancers	Rectal Smooth Muscle	rectum
45	chr9:100293800-100294000	Enhancers	Stomach Smooth Muscle	stomach
46	chr9:100293800-100294600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:100293800-100294800	Enhancers	Brain Anterior Caudate	brain
48	chr9:100293800-100294800	Enhancers	Left Ventricle	heart
49	chr9:100293800-100294800	Genic enhancers	HSMMtube	muscle
50	chr9:100293800-100295000	Enhancers	Psoas Muscle	Psoas

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