Variant report

Variant	esv2830205
Chromosome Location	chr10:51978430-52135215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2472)
CpG islands
(count:549)
Chromatin interactive
region (count:112)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:2472 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52051151-52051887	K562	blood:	n/a	chr10:52051843-52051859
2	ARID3A	chr10:52035412-52035803	K562	blood:	n/a	n/a
3	ARID3A	chr10:52124449-52124686	K562	blood:	n/a	n/a
4	ARID3A	chr10:52096785-52097419	K562	blood:	n/a	n/a
5	ARID3A	chr10:52132787-52132975	K562	blood:	n/a	n/a
6	ARID3A	chr10:52091151-52092344	K562	blood:	n/a	n/a
7	ARID3A	chr10:52063453-52063845	K562	blood:	n/a	n/a
8	ARID3A	chr10:52070534-52070946	K562	blood:	n/a	n/a
9	ARID3A	chr10:52075129-52075588	K562	blood:	n/a	n/a
10	ARID3A	chr10:52011227-52011506	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:52077960-52078184	K562	blood:	n/a	n/a
12	ARID3A	chr10:52072531-52073538	K562	blood:	n/a	n/a
13	ARID3A	chr10:52099381-52099787	K562	blood:	n/a	n/a
14	ARID3A	chr10:52120334-52120358	K562	blood:	n/a	n/a
15	ARID3A	chr10:52078573-52079065	K562	blood:	n/a	n/a
16	ARID3A	chr10:52020838-52021159	HepG2	liver:	n/a	n/a
17	ARID3A	chr10:52127535-52127844	K562	blood:	n/a	n/a
18	ARID3A	chr10:52117735-52118515	K562	blood:	n/a	n/a
19	ARID3A	chr10:52081241-52082196	K562	blood:	n/a	n/a
20	ARID3A	chr10:52111590-52111825	K562	blood:	n/a	n/a
21	ARID3A	chr10:52084484-52089746	K562	blood:	n/a	chr10:52089059-52089075 chr10:52089058-52089074
22	ARID3A	chr10:52055144-52055451	K562	blood:	n/a	n/a
23	ARID3A	chr10:52090227-52090559	K562	blood:	n/a	n/a
24	ARID3A	chr10:51994435-51994634	HepG2	liver:	n/a	n/a
25	ARID3A	chr10:52076596-52077385	K562	blood:	n/a	n/a
26	ATF1	chr10:52020533-52020905	K562	blood:	n/a	n/a
27	ATF1	chr10:52072566-52073079	K562	blood:	n/a	n/a
28	ATF1	chr10:52086523-52087559	K562	blood:	n/a	n/a
29	ATF1	chr10:52085140-52085785	K562	blood:	n/a	n/a
30	ATF2	chr10:52020470-52020997	GM12878	blood:	n/a	n/a
31	ATF2	chr10:52122262-52123094	GM12878	blood:	n/a	n/a
32	ATF2	chr10:52134583-52135111	GM12878	blood:	n/a	n/a
33	ATF2	chr10:52085076-52085573	GM12878	blood:	n/a	n/a
34	ATF2	chr10:52106973-52107749	GM12878	blood:	n/a	n/a
35	ATF2	chr10:52122180-52122928	GM12878	blood:	n/a	n/a
36	ATF2	chr10:52107026-52107665	GM12878	blood:	n/a	n/a
37	ATF2	chr10:52020317-52021056	GM12878	blood:	n/a	n/a
38	ATF3	chr10:52086482-52087108	K562	blood:	n/a	n/a
39	ATF3	chr10:52085055-52085796	K562	blood:	n/a	n/a
40	BACH1	chr10:52091726-52092287	K562	blood:	n/a	n/a
41	BACH1	chr10:52086440-52087663	K562	blood:	n/a	n/a
42	BACH1	chr10:52079541-52079637	K562	blood:	n/a	n/a
43	BACH1	chr10:52039370-52039740	K562	blood:	n/a	chr10:52039520-52039534
44	BACH1	chr10:52035377-52035783	K562	blood:	n/a	n/a
45	BACH1	chr10:52100879-52101325	K562	blood:	n/a	n/a
46	BACH1	chr10:52039339-52039690	H1-hESC	embryonic stem cell:	n/a	chr10:52039520-52039534
47	BACH1	chr10:52035455-52035788	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr10:52073601-52073850	K562	blood:	n/a	n/a
49	BACH1	chr10:52092573-52092805	K562	blood:	n/a	n/a
50	BACH1	chr10:52125123-52125148	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52115183-52115233	LNCaP	prostate:	n/a
2	chr10:52002547-52002597	AoSMC	blood vessel:	n/a
3	chr10:52008593-52008643	U87	brain:	n/a
4	chr10:52115183-52115233	BE2_C	brain:	n/a
5	chr10:52066867-52066917	Caco-2	colon:	n/a
6	chr10:52008805-52008855	HMEC	breast:	n/a
7	chr10:52008360-52008410	AoSMC	blood vessel:	n/a
8	chr10:52008360-52008410	HEEpiC	esophagus:	n/a
9	chr10:52008905-52008955	H1-hESC	embryonic stem cell:	embryo
10	chr10:52115682-52115732	SK-N-SH	brain:	n/a
11	chr10:52115183-52115233	ProgFib	skin:	n/a
12	chr10:52008360-52008410	MCF-7	breast:	n/a
13	chr10:52115682-52115732	HCPEpiC	choroid plexus:	n/a
14	chr10:52008905-52008955	HAEpiC	amniotic membrane:	n/a
15	chr10:52115682-52115732	HUVEC	blood vessel:	n/a
16	chr10:52008905-52008955	HNPCEpiC	eye:	n/a
17	chr10:52008805-52008855	PANC-1	pancreas:	n/a
18	chr10:52008805-52008855	HCM	heart:	n/a
19	chr10:52008360-52008410	U87	brain:	n/a
20	chr10:52008905-52008955	NHBE	bronchial:	n/a
21	chr10:52008905-52008955	Caco-2	colon:	n/a
22	chr10:52008593-52008643	HUVEC	blood vessel:	n/a
23	chr10:52008905-52008955	ECC-1	luminal epithelium:	n/a
24	chr10:52008805-52008855	NHBE	bronchial:	n/a
25	chr10:52008805-52008855	HepG2	liver:	n/a
26	chr10:52008360-52008410	T-47D	breast:	n/a
27	chr10:52008593-52008643	PrEC	prostate:	n/a
28	chr10:52120283-52120333	A549	lung:	n/a
29	chr10:52120283-52120333	U87	brain:	n/a
30	chr10:52115682-52115732	MCF10A-Er-Src	breast:	n/a
31	chr10:52115183-52115233	AG04450	lung:	fetal
32	chr10:52115682-52115732	NHDF-neo	bronchial:	n/a
33	chr10:52066867-52066917	LNCaP	prostate:	n/a
34	chr10:52002547-52002597	HCM	heart:	n/a
35	chr10:52008805-52008855	NT2-D1	testis:	n/a
36	chr10:52008593-52008643	NH-A	brain:	n/a
37	chr10:52115183-52115233	HCF	heart:	n/a
38	chr10:52115682-52115732	GM12892	blood:	n/a
39	chr10:52008805-52008855	ECC-1	luminal epithelium:	n/a
40	chr10:52008805-52008855	H1-hESC	embryonic stem cell:	embryo
41	chr10:52115183-52115233	Hela-S3	cervix:	n/a
42	chr10:52008593-52008643	H1-hESC	embryonic stem cell:	embryo
43	chr10:52008805-52008855	GM12878	blood:	n/a
44	chr10:52066867-52066917	HMEC	breast:	n/a
45	chr10:52120283-52120333	K562	blood:	n/a
46	chr10:52115183-52115233	SK-N-MC	brain:	n/a
47	chr10:52008905-52008955	K562	blood:	n/a
48	chr10:52120283-52120333	HUVEC	blood vessel:	n/a
49	chr10:52008805-52008855	IMR90	lung:	fetal
50	chr10:52115183-52115233	HAEpiC	amniotic membrane:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
2	chr10:52087443..52089388-chr10:52116523..52119614,3	K562	blood:
3	chr10:52014263..52015864-chr10:52038453..52040858,2	K562	blood:
4	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
5	chr10:52118184..52120411-chr10:52292971..52295430,2	K562	blood:
6	chr10:52029815..52033760-chr10:52034548..52037259,4	K562	blood:
7	chr10:52103151..52105270-chr10:52383748..52386662,2	K562	blood:
8	chr10:52109231..52111670-chr10:52122633..52124290,2	K562	blood:
9	chr10:52063071..52064625-chr10:52072402..52074193,2	MCF-7	breast:
10	chr10:52132819..52134741-chr10:52135257..52137397,2	K562	blood:
11	chr10:52053125..52055994-chr10:52093315..52095681,2	K562	blood:
12	chr10:52125875..52128899-chr10:52129822..52132966,4	K562	blood:
13	chr10:52039584..52041526-chr10:52044440..52046214,2	MCF-7	breast:
14	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
15	chr10:52033462..52036031-chr10:52039236..52041874,2	K562	blood:
16	chr10:52050788..52053473-chr10:52085482..52088054,2	K562	blood:
17	chr10:52120330..52124092-chr10:52125493..52129232,4	K562	blood:
18	chr10:52011614..52013335-chr10:52018420..52020373,2	K562	blood:
19	chr10:52131563..52133207-chr10:52144228..52146255,2	K562	blood:
20	chr10:52046559..52050186-chr10:52057567..52060183,3	K562	blood:
21	chr10:52100945..52103388-chr10:52103997..52106988,2	MCF-7	breast:
22	chr10:52065089..52067181-chr10:52085442..52087556,2	K562	blood:
23	chr10:52009441..52011844-chr10:52036005..52038580,2	K562	blood:
24	chr10:52084222..52086810-chr10:52173871..52176505,2	K562	blood:
25	chr10:52036642..52039011-chr10:52040195..52041719,2	K562	blood:
26	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
27	chr10:52064687..52067489-chr10:52072620..52075726,3	K562	blood:
28	chr10:52071869..52074741-chr10:52080323..52082329,2	MCF-7	breast:
29	chr10:52043739..52044593-chr2:55242128..55242713,2	K562	blood:
30	chr10:52065089..52067181-chr10:52085442..52087556,2	K562	blood:
31	chr10:52047341..52049235-chr10:52083279..52085507,2	K562	blood:
32	chr10:52091344..52092956-chr10:52110761..52113396,2	MCF-7	breast:
33	chr10:52085312..52087982-chr10:52138618..52141238,2	K562	blood:
34	chr10:52050788..52053473-chr10:52085482..52088054,2	K562	blood:
35	chr10:52032843..52037067-chr10:52037860..52041874,6	K562	blood:
36	chr10:52033462..52036031-chr10:52039236..52041874,2	K562	blood:
37	chr10:52034197..52036639-chr10:52176402..52178569,2	K562	blood:
38	chr10:52084925..52086838-chr10:52120229..52123147,2	K562	blood:
39	chr10:52120816..52123329-chr10:52287278..52290056,2	MCF-7	breast:
40	chr10:52091344..52092956-chr10:52110761..52113396,2	MCF-7	breast:
41	chr10:52044776..52046727-chr10:52383268..52385118,2	K562	blood:
42	chr10:52125875..52128899-chr10:52129822..52132966,4	K562	blood:
43	chr10:52127277..52127980-chr10:52180802..52181438,3	MCF-7	breast:
44	chr10:52040531..52043332-chr10:52062739..52065495,2	K562	blood:
45	chr10:52087443..52089388-chr10:52116523..52119614,3	K562	blood:
46	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
47	chr10:52115339..52118395-chr10:52119759..52122908,4	K562	blood:
48	chr10:52040531..52043332-chr10:52062739..52065495,2	K562	blood:
49	chr10:52089314..52090958-chr10:52289108..52291926,2	K562	blood:
50	chr10:52029815..52033760-chr10:52034548..52037259,4	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM21A-2	chr10:52062175-52063940	l_311_chr10:52061403-52063940_testes
2	lnc-ASAH2-5	chr10:52104168-52104349	l_312_chr10:52096258-52104698_testes
3	lnc-ASAH2-5	chr10:52096259-52096435	l_312_chr10:52096258-52104698_testes
4	lnc-FAM21A-2	chr10:52061404-52061522	l_311_chr10:52061403-52063940_testes
5	lnc-ASAH2-4	chr10:52102202-52102561	NONHSAT013378
6	lnc-ASAH2-5	chr10:52104608-52104698	l_312_chr10:52096258-52104698_testes
7	lnc-ASAH2-5	chr10:52096448-52096864	l_312_chr10:52096258-52104698_testes
8	lnc-ASAH2-6	chr10:52103896-52104105	NONHSAT013379

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SGMS1	hsa-miR-130b-3p	chr10:52066406-52066429
2	SGMS1	hsa-miR-124-3p	chr10:52066157-52066151
3	SGMS1	hsa-miR-33a-5p	chr10:52066188-52066208
4	SGMS1	hsa-miR-130b-3p	chr10:52066046-52066067
5	SGMS1	hsa-miR-124-3p	chr10:52066151-52066170
6	SGMS1	hsa-miR-130b-3p	chr10:52066686-52066707
7	SGMS1	hsa-miR-130b-3p	chr10:52065388-52065411
8	SGMS1	hsa-miR-93-5p	chr10:52065386-52065408
9	SGMS1	hsa-miR-33a-5p	chr10:52065390-52065409

Variant related genes	Relation type
SGMS1	TF binding region
ENSG00000269165	TF binding region
DYNC1I2P1	TF binding region
ASAH2	TF binding region
SGMS1	CpG island
ENSG00000269165	CpG island
DYNC1I2P1	CpG island
ASAH2	CpG island
ENSG00000269165	chromatin interactions
ENSG00000188611	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000198964	chromatin interactions

Extended variants
information (count: 4853 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4853 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547681820	chr10:52000006-52000007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200608523	chr10:52000164-52000165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201940528	chr10:52000233-52000234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570850351	chr10:52000259-52000260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538232812	chr10:52000279-52000280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558158802	chr10:52000280-52000281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568859058	chr10:52000281-52000282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537511977	chr10:52000533-52000534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7902744	chr10:52000536-52000537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574502641	chr10:52000592-52000593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540470573	chr10:52000813-52000814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73320289	chr10:52000840-52000841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141568509	chr10:52000907-52000908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546139216	chr10:52000919-52000920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150912922	chr10:52000968-52000969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs66941844	chr10:52000999-52001000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541911774	chr10:52001019-52001020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562256623	chr10:52001026-52001027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527872473	chr10:52001075-52001076	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs190475293	chr10:52001080-52001081	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs139482707	chr10:52001096-52001097	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182255923	chr10:52001129-52001130	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs144209627	chr10:52001155-52001156	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568721286	chr10:52001221-52001222	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs184579702	chr10:52001300-52001301	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs12267073	chr10:52001303-52001304	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536461135	chr10:52001330-52001331	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs188897580	chr10:52001367-52001368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs553979128	chr10:52001389-52001390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs570335076	chr10:52001414-52001415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577125613	chr10:52001447-52001448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546078433	chr10:52001449-52001450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374220186	chr10:52001463-52001464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146078683	chr10:52001466-52001467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576354531	chr10:52001480-52001481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542249329	chr10:52001481-52001482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562026341	chr10:52001495-52001496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572236800	chr10:52001496-52001497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541150890	chr10:52001503-52001504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564307666	chr10:52001585-52001586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533359527	chr10:52001600-52001601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550018640	chr10:52001627-52001628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368419518	chr10:52001637-52001638	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12258578	chr10:52001645-52001646	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548194039	chr10:52001702-52001703	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567983993	chr10:52001736-52001737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574305806	chr10:52001738-52001739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12258643	chr10:52001789-52001790	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181595796	chr10:52001804-52001805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs76544369	chr10:52001906-52001907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2203 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52000000-52002000	Weak transcription	Fetal Intestine Small	intestine
2	chr10:52000000-52003000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr10:52002000-52002200	Strong transcription	Fetal Intestine Small	intestine
4	chr10:52002200-52002400	Bivalent Enhancer	K562	blood
5	chr10:52002200-52002800	Weak transcription	Fetal Intestine Small	intestine
6	chr10:52002400-52003800	Enhancers	K562	blood
7	chr10:52002800-52003000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:52002800-52003000	Bivalent Enhancer	A549	lung
9	chr10:52002800-52003800	Strong transcription	Fetal Intestine Small	intestine
10	chr10:52003000-52003200	Enhancers	Duodenum Mucosa	Duodenum
11	chr10:52003000-52005200	Enhancers	Fetal Intestine Large	intestine
12	chr10:52003200-52003600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr10:52003600-52004400	Enhancers	Duodenum Mucosa	Duodenum
14	chr10:52003800-52004200	Bivalent Enhancer	K562	blood
15	chr10:52003800-52005200	Genic enhancers	Fetal Intestine Small	intestine
16	chr10:52003800-52005200	Enhancers	Small Intestine	intestine
17	chr10:52004000-52004600	Enhancers	HepG2	liver
18	chr10:52004400-52006600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr10:52004600-52007400	Weak transcription	HepG2	liver
20	chr10:52005200-52006400	Weak transcription	Fetal Intestine Small	intestine
21	chr10:52005200-52007200	Weak transcription	Fetal Intestine Large	intestine
22	chr10:52005200-52007600	Weak transcription	Small Intestine	intestine
23	chr10:52006400-52006600	Enhancers	Fetal Intestine Small	intestine
24	chr10:52006600-52007000	Weak transcription	Fetal Intestine Small	intestine
25	chr10:52006600-52007600	Enhancers	Duodenum Mucosa	Duodenum
26	chr10:52007000-52008800	Enhancers	Fetal Intestine Small	intestine
27	chr10:52007200-52009600	Enhancers	Fetal Intestine Large	intestine
28	chr10:52007400-52010000	Enhancers	HepG2	liver
29	chr10:52007400-52010200	Enhancers	Liver	Liver
30	chr10:52007600-52007800	Enhancers	Small Intestine	intestine
31	chr10:52007600-52009000	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr10:52007800-52008200	Enhancers	Stomach Mucosa	stomach
33	chr10:52008600-52009000	Bivalent Enhancer	Small Intestine	intestine
34	chr10:52008800-52009000	Flanking Active TSS	Fetal Intestine Small	intestine
35	chr10:52009000-52009400	Enhancers	Fetal Intestine Small	intestine
36	chr10:52009000-52010000	Enhancers	Duodenum Mucosa	Duodenum
37	chr10:52009400-52010200	Flanking Active TSS	Fetal Intestine Small	intestine
38	chr10:52009600-52010000	Flanking Active TSS	Fetal Intestine Large	intestine
39	chr10:52010000-52010200	Flanking Active TSS	Duodenum Mucosa	Duodenum
40	chr10:52010000-52010400	Active TSS	Fetal Intestine Large	intestine
41	chr10:52010000-52011600	Flanking Active TSS	HepG2	liver
42	chr10:52010200-52010400	Active TSS	Fetal Intestine Small	intestine
43	chr10:52010200-52010600	Flanking Active TSS	Liver	Liver
44	chr10:52010200-52010600	Active TSS	Duodenum Mucosa	Duodenum
45	chr10:52010200-52011400	Enhancers	K562	blood
46	chr10:52010400-52010600	Flanking Active TSS	Fetal Intestine Small	intestine
47	chr10:52010400-52011400	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr10:52010600-52010800	Active TSS	Fetal Intestine Small	intestine
49	chr10:52010600-52011400	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr10:52010600-52011800	Enhancers	Liver	Liver

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