Variant report

Variant	nsv877687
Chromosome Location	chr3:156924793-157044184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:901)
CpG islands
(count:306)
Chromatin interactive
region (count:58)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:157018694-157019077	K562	blood:	n/a	n/a
2	ARID3A	chr3:156956919-156957202	K562	blood:	n/a	n/a
3	ARID3A	chr3:157024078-157024080	K562	blood:	n/a	n/a
4	ARID3A	chr3:156938825-156939003	HepG2	liver:	n/a	n/a
5	ATF1	chr3:157003905-157004091	K562	blood:	n/a	n/a
6	ATF1	chr3:157011888-157012028	K562	blood:	n/a	n/a
7	ATF1	chr3:156997015-156997407	K562	blood:	n/a	n/a
8	ATF1	chr3:156966409-156966734	K562	blood:	n/a	n/a
9	ATF1	chr3:157018663-157019087	K562	blood:	n/a	n/a
10	ATF3	chr3:157019000-157019374	K562	blood:	n/a	n/a
11	ATF3	chr3:156966352-156966669	K562	blood:	n/a	n/a
12	BACH1	chr3:156943175-156943179	K562	blood:	n/a	n/a
13	BATF	chr3:156944008-156944231	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:156990271-156990449	K562	blood:	n/a	n/a
15	BHLHE40	chr3:157018775-157019084	K562	blood:	n/a	n/a
16	BHLHE40	chr3:156956925-156957209	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:157000010-157000637	K562	blood:	n/a	n/a
18	BHLHE40	chr3:156956971-156957199	K562	blood:	n/a	n/a
19	BRCA1	chr3:157011833-157011877	Hela-S3	cervix:	n/a	n/a
20	CCNT2	chr3:156966530-156966744	K562	blood:	n/a	n/a
21	CCNT2	chr3:157018743-157019140	K562	blood:	n/a	n/a
22	CEBPB	chr3:156938812-156938863	A549	lung:	n/a	chr3:156938838-156938849
23	CEBPB	chr3:157019041-157019366	A549	lung:	n/a	chr3:157019202-157019213
24	CEBPB	chr3:156975070-156975293	K562	blood:	n/a	n/a
25	CEBPB	chr3:157008590-157008976	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:156926067-156926244	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:157018799-157019699	K562	blood:	n/a	chr3:157019202-157019213
28	CEBPB	chr3:157019074-157019368	H1-hESC	embryonic stem cell:	n/a	chr3:157019202-157019213
29	CEBPB	chr3:157019020-157019377	IMR90	lung:	n/a	chr3:157019202-157019213
30	CEBPB	chr3:157029426-157029958	ECC-1	luminal epithelium:	n/a	chr3:157029742-157029753
31	CEBPB	chr3:157029400-157030538	Hela-S3	cervix:	n/a	chr3:157029742-157029753
32	CEBPB	chr3:156975029-156975242	H1-hESC	embryonic stem cell:	n/a	chr3:156975048-156975060
33	CEBPB	chr3:157010802-157011028	A549	lung:	n/a	chr3:157010885-157010896 chr3:157010885-157010898 chr3:157010887-157010896 chr3:157010887-157010896 chr3:157010885-157010898 chr3:157010885-157010896 chr3:157010887-157010896 chr3:157010885-157010898 chr3:157010887-157010896 chr3:157010886-157010897
34	CEBPB	chr3:157019118-157019332	K562	blood:	n/a	chr3:157019202-157019213
35	CEBPB	chr3:156953122-156953446	K562	blood:	n/a	n/a
36	CEBPB	chr3:157029439-157029981	A549	lung:	n/a	chr3:157029742-157029753
37	CEBPB	chr3:156999911-157000804	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:157029478-157029918	K562	blood:	n/a	chr3:157029742-157029753
39	CEBPB	chr3:156965129-156965371	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:157029470-157029910	HepG2	liver:	n/a	chr3:157029742-157029753
41	CEBPB	chr3:157023317-157023593	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:156957004-156957204	K562	blood:	n/a	n/a
43	CEBPB	chr3:157019032-157019758	Hela-S3	cervix:	n/a	chr3:157019202-157019213
44	CEBPB	chr3:156975053-156975311	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:156925961-156926145	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:157018744-157019457	K562	blood:	n/a	chr3:157019202-157019213
47	CEBPB	chr3:156943996-156944356	IMR90	lung:	n/a	chr3:156944166-156944177 chr3:156944166-156944179 chr3:156944166-156944179
48	CEBPB	chr3:157029478-157029872	MCF-7	breast:	n/a	chr3:157029742-157029753
49	CEBPB	chr3:157010760-157011039	IMR90	lung:	n/a	chr3:157010885-157010896 chr3:157010885-157010898 chr3:157010887-157010896 chr3:157010887-157010896 chr3:157010885-157010898 chr3:157010885-157010896 chr3:157010887-157010896 chr3:157010885-157010898 chr3:157010887-157010896 chr3:157010886-157010897
50	CEBPB	chr3:157029425-157030327	IMR90	lung:	n/a	chr3:157029742-157029753

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:156955923-156955973	HAEpiC	amniotic membrane:	n/a
2	chr3:156955923-156955973	HAEpiC	amniotic membrane:	n/a
3	chr3:156975045-156975095	AG04450	lung:	fetal
4	chr3:156975045-156975095	HCPEpiC	choroid plexus:	n/a
5	chr3:156977642-156977692	AG09319	gingival:	n/a
6	chr3:156967557-156967607	ProgFib	skin:	n/a
7	chr3:156966620-156966670	HNPCEpiC	eye:	n/a
8	chr3:156977642-156977692	NT2-D1	testis:	n/a
9	chr3:156955923-156955973	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:156977642-156977692	HCF	heart:	n/a
11	chr3:156967557-156967607	GM12892	blood:	n/a
12	chr3:156967557-156967607	AG04449	skin:	fetal
13	chr3:156955923-156955973	HRCEpiC	kidney:	n/a
14	chr3:156955923-156955973	MCF10A-Er-Src	breast:	n/a
15	chr3:156977642-156977692	GM12891	blood:	n/a
16	chr3:156977642-156977692	HMEC	breast:	n/a
17	chr3:156975045-156975095	AoSMC	blood vessel:	n/a
18	chr3:156975045-156975095	AG10803	skin:	n/a
19	chr3:156977642-156977692	CMK	blood:	n/a
20	chr3:156966620-156966670	ProgFib	skin:	n/a
21	chr3:156975045-156975095	SK-N-MC	brain:	n/a
22	chr3:156975045-156975095	MCF-7	breast:	n/a
23	chr3:156975045-156975095	SKMC	muscle:	n/a
24	chr3:156966620-156966670	GM19239	blood:	n/a
25	chr3:156955923-156955973	SKMC	muscle:	n/a
26	chr3:156955923-156955973	T-47D	breast:	n/a
27	chr3:156966620-156966670	Hela-S3	cervix:	n/a
28	chr3:156967557-156967607	IMR90	lung:	fetal
29	chr3:156955923-156955973	SK-N-SH	brain:	n/a
30	chr3:156977642-156977692	HEK293	kidney:	embryo
31	chr3:156955923-156955973	NHDF-neo	bronchial:	n/a
32	chr3:156967557-156967607	HRE	kidney:	n/a
33	chr3:156975045-156975095	Hepatocyte	liver:	n/a
34	chr3:156977642-156977692	HepG2	liver:	n/a
35	chr3:156966620-156966670	HCPEpiC	choroid plexus:	n/a
36	chr3:156975045-156975095	ovcar-3	ovarian:	n/a
37	chr3:156967557-156967607	SAEC	small airway:	n/a
38	chr3:156967557-156967607	PFSK-1	brain:	n/a
39	chr3:156977642-156977692	HCT-116	colon:	n/a
40	chr3:156967557-156967607	K562	blood:	n/a
41	chr3:156955923-156955973	HRE	kidney:	n/a
42	chr3:156977642-156977692	GM12878	blood:	n/a
43	chr3:156966620-156966670	GM12878	blood:	n/a
44	chr3:156955923-156955973	AG10803	skin:	n/a
45	chr3:156975045-156975095	HL-60	blood:	n/a
46	chr3:156975045-156975095	A549	lung:	n/a
47	chr3:156977642-156977692	GM19239	blood:	n/a
48	chr3:156966620-156966670	AG09309	skin:	n/a
49	chr3:156975045-156975095	PANC-1	pancreas:	n/a
50	chr3:156977642-156977692	U87	brain:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:12407968..12410146-chr3:156930881..156932746,2	MCF-7	breast:
2	chr3:156876704..156879523-chr3:156929724..156931977,2	MCF-7	breast:
3	chr3:157022820..157026060-chr3:157027403..157031164,3	K562	blood:
4	chr3:157022820..157026060-chr3:157027403..157031164,3	K562	blood:
5	chr3:156921948..156922690-chr3:156957018..156957556,2	MCF-7	breast:
6	chr3:156869339..156870911-chr3:156949584..156952069,2	K562	blood:
7	chr3:156937140..156939016-chr3:156942989..156946437,3	MCF-7	breast:
8	chr3:156898169..156900911-chr3:156944162..156945884,2	K562	blood:
9	chr3:157027546..157030155-chr3:157033829..157035547,2	K562	blood:
10	chr3:156976265..156978108-chr3:156979247..156980892,2	MCF-7	breast:
11	chr3:156956612..156957498-chr3:157211529..157212391,2	MCF-7	breast:
12	chr3:156943575..156945121-chr3:156948800..156950615,2	K562	blood:
13	chr3:156951228..156953656-chr3:157037881..157040326,2	MCF-7	breast:
14	chr3:156901238..156905299-chr3:156943501..156945279,3	K562	blood:
15	chr3:157005885..157009539-chr3:157009923..157012607,4	K562	blood:
16	chr3:157008081..157011337-chr3:157013720..157016384,3	K562	blood:
17	chr3:156889937..156892577-chr3:156953909..156956061,2	K562	blood:
18	chr3:156875949..156879097-chr3:156957620..156960607,3	K562	blood:
19	chr3:156999731..157001800-chr3:157004485..157007413,2	MCF-7	breast:
20	chr3:156988336..156991271-chr3:156994407..156996753,2	K562	blood:
21	chr3:156920987..156922623-chr3:156924558..156927431,2	K562	blood:
22	chr3:156876962..156878616-chr3:156936583..156938253,2	K562	blood:
23	chr3:157027546..157030155-chr3:157033829..157035547,2	K562	blood:
24	chr3:156950469..156951990-chr3:156955060..156957422,2	K562	blood:
25	chr3:157008081..157011337-chr3:157013720..157016384,3	K562	blood:
26	chr3:156918691..156919685-chr3:156957052..156957552,2	K562	blood:
27	chr3:156914056..156915749-chr3:156927497..156930376,2	K562	blood:
28	chr3:156950469..156951990-chr3:156955060..156957422,2	K562	blood:
29	chr3:156997473..157000192-chr3:157001265..157003413,2	K562	blood:
30	chr3:156999731..157001800-chr3:157004485..157007413,2	MCF-7	breast:
31	chr3:157007024..157009748-chr3:157011757..157013274,2	MCF-7	breast:
32	chr3:156933862..156936263-chr3:156942374..156944793,2	K562	blood:
33	chr3:156933862..156936263-chr3:156942374..156944793,2	K562	blood:
34	chr3:156957752..156961185-chr3:156962599..156965057,3	K562	blood:
35	chr3:156876126..156877754-chr3:156933558..156935283,2	K562	blood:
36	chr3:156951228..156953656-chr3:157037881..157040326,2	MCF-7	breast:
37	chr3:156974074..156978072-chr3:156979844..156983022,4	K562	blood:
38	chr3:157001018..157003742-chr3:157209899..157211507,2	K562	blood:
39	chr3:156876934..156879709-chr3:156982846..156986882,3	K562	blood:
40	chr3:156974074..156978072-chr3:156979844..156983022,4	K562	blood:
41	chr3:156976265..156978108-chr3:156979247..156980892,2	MCF-7	breast:
42	chr3:156987878..156990782-chr3:156994349..156996892,2	MCF-7	breast:
43	chr3:156957752..156961185-chr3:156962599..156965057,3	K562	blood:
44	chr3:156937140..156939016-chr3:156942989..156946437,3	MCF-7	breast:
45	chr3:156987878..156990782-chr3:156994349..156996892,2	MCF-7	breast:
46	chr3:156872209..156874500-chr3:156943435..156945429,2	K562	blood:
47	chr3:156921859..156922577-chr3:156956944..156957575,2	MCF-7	breast:
48	chr3:157005885..157009539-chr3:157009923..157012607,4	K562	blood:
49	chr3:156928672..156931492-chr3:157212092..157213882,2	MCF-7	breast:
50	chr3:156875663..156878601-chr3:156956786..156959531,4	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LEKR1-4	chr3:156957379-156957753	ENSG00000243176.1
2	lnc-LEKR1-4	chr3:157004061-157004130	ENSG00000243176.1
3	lnc-LEKR1-4	chr3:156957379-156957588	ENSG00000243176.1
4	lnc-LEKR1-4	chr3:157033600-157033934	ENSG00000243176.1
5	lnc-LEKR1-4	chr3:156948068-156948086	ENSG00000243176.1
6	lnc-LEKR1-4	chr3:157001013-157001078	NONHSAT092913
7	lnc-LEKR1-4	chr3:156957396-156957588	NONHSAT092913
8	lnc-LEKR1-4	chr3:157003949-157004130	ENSG00000243176.1
9	lnc-CCNL1-6	chr3:157024986-157025211	expReg_chr3_11171_-
10	lnc-LEKR1-4	chr3:156957379-156957588	ENSG00000243176.1
11	lnc-LEKR1-4	chr3:156957379-156957588	ENSG00000243176.1
12	lnc-LEKR1-4	chr3:156951400-156951409	NONHSAT092912
13	lnc-LEKR1-4	chr3:156957379-156957578	NONHSAT092912
14	lnc-LEKR1-4	chr3:157033600-157033684	ENSG00000243176.1
15	lnc-VEPH1-1	chr3:156948109-156948997	NONHSAT092911
16	lnc-CCNL1-4	chr3:156953714-156953883	NONHSAT092909
17	lnc-CCNL1-4	chr3:156929228-156929521	NONHSAT092909
18	lnc-LEKR1-4	chr3:157002767-157003080	ENSG00000243176.1

No data

Variant related genes	Relation type
ENSG00000243176	TF binding region
ENSG00000270981	TF binding region
ENSG00000243176	CpG island
ENSG00000270981	CpG island
ENSG00000174899	chromatin interactions
ENSG00000222675	chromatin interactions
ENSG00000197415	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000270981	chromatin interactions

Extended variants
information (count: 4010 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4010 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12634818	chr3:156924793-156924794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374063935	chr3:156924826-156924827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62276490	chr3:156924838-156924839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs531603947	chr3:156924914-156924915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543458065	chr3:156924916-156924917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543462548	chr3:156924917-156924918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs62276491	chr3:156924966-156924967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532705187	chr3:156924981-156924982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547659556	chr3:156925000-156925001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529363739	chr3:156925001-156925002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530320744	chr3:156925246-156925247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75319622	chr3:156925272-156925273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569624393	chr3:156925298-156925299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55953639	chr3:156925305-156925306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs558654651	chr3:156925322-156925323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574575356	chr3:156925355-156925356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570440964	chr3:156925370-156925371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56825034	chr3:156925399-156925400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200321141	chr3:156925408-156925409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199808098	chr3:156925411-156925412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534745711	chr3:156925420-156925421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377609931	chr3:156925441-156925442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139078003	chr3:156925453-156925454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541679712	chr3:156925455-156925456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149958121	chr3:156925465-156925466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368031058	chr3:156925471-156925472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543427902	chr3:156925473-156925474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565315459	chr3:156925487-156925488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532476973	chr3:156925511-156925512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541559776	chr3:156925630-156925631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559651803	chr3:156925706-156925707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530322752	chr3:156925707-156925708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117421515	chr3:156925744-156925745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570378385	chr3:156925770-156925771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551947110	chr3:156925800-156925801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531268501	chr3:156925834-156925835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71310496	chr3:156925857-156925858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552183047	chr3:156925870-156925871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570476776	chr3:156925876-156925877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534412345	chr3:156925878-156925879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546682203	chr3:156925903-156925904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182010082	chr3:156925957-156925958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535285806	chr3:156926090-156926091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147225726	chr3:156926231-156926232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545766098	chr3:156926237-156926238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575176830	chr3:156926281-156926282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568335416	chr3:156926282-156926283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111755539	chr3:156926284-156926285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558676545	chr3:156926289-156926290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367799640	chr3:156926348-156926349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156919400-156929000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr3:156919600-156928800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr3:156920200-156929600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr3:156922200-156925000	Enhancers	Osteobl	bone
5	chr3:156923000-156927400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr3:156923200-156925000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr3:156923400-156924800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:156923400-156926400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:156923400-156927400	Weak transcription	Fetal Stomach	stomach
10	chr3:156923400-156928600	Weak transcription	Colon Smooth Muscle	Colon
11	chr3:156923800-156928400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr3:156924400-156925200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:156924400-156934000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr3:156924600-156925000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:156924600-156925000	Enhancers	NHDF-Ad	bronchial
16	chr3:156924800-156925200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr3:156925000-156929200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr3:156925400-156927000	Weak transcription	Primary T cells from cord blood	blood
19	chr3:156925600-156928000	Weak transcription	Pancreas	Pancrea
20	chr3:156926000-156926600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:156926200-156928600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr3:156926400-156926600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:156926400-156926800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:156926400-156926800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:156926600-156927400	Enhancers	HepG2	liver
26	chr3:156926600-156928800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:156926600-156929000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr3:156926800-156927200	Enhancers	Liver	Liver
29	chr3:156926800-156927800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:156926800-156928000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:156927000-156927600	Strong transcription	Primary T cells from cord blood	blood
32	chr3:156927600-156934400	Weak transcription	Primary T cells from cord blood	blood
33	chr3:156927800-156928000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr3:156927800-156928200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:156928000-156928400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:156928000-156928400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:156928000-156928600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:156928000-156928800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr3:156928200-156928800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:156928400-156928600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr3:156928800-156929000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:156929200-156929600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:156929200-156929800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:156934000-156934400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr3:156936600-156937400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:156937000-156937200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:156937000-156938200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:156937200-156938000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:156937400-156938400	Enhancers	Osteobl	bone
50	chr3:156937800-156938800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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