Variant report

Variant	esv3448813
Chromosome Location	chr10:43919995-43950867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1453)
CpG islands
(count:917)
Chromatin interactive
region (count:76)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1453 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43926756-43926757	K562	blood:	n/a	n/a
2	ARID3A	chr10:43926083-43926102	K562	blood:	n/a	n/a
3	ARID3A	chr10:43931785-43932602	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:43932036-43932352	K562	blood:	n/a	n/a
5	ARID3A	chr10:43950818-43951624	K562	blood:	n/a	n/a
6	ARID3A	chr10:43950776-43951450	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:43949958-43950398	K562	blood:	n/a	chr10:43950094-43950110 chr10:43950095-43950111
8	ATF1	chr10:43950793-43951427	K562	blood:	n/a	n/a
9	ATF1	chr10:43931757-43932586	K562	blood:	n/a	n/a
10	ATF2	chr10:43948773-43949301	GM12878	blood:	n/a	n/a
11	ATF2	chr10:43950720-43951447	GM12878	blood:	n/a	n/a
12	ATF2	chr10:43947310-43947971	GM12878	blood:	n/a	n/a
13	ATF2	chr10:43948851-43949227	GM12878	blood:	n/a	n/a
14	ATF3	chr10:43950805-43951586	K562	blood:	n/a	n/a
15	ATF3	chr10:43932056-43932580	K562	blood:	n/a	n/a
16	ATF3	chr10:43950811-43951427	A549	lung:	n/a	n/a
17	BACH1	chr10:43950843-43951508	K562	blood:	n/a	n/a
18	BACH1	chr10:43950720-43951472	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:43932821-43932825	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr10:43948829-43949229	GM12878	blood:	n/a	n/a
21	BATF	chr10:43948888-43949178	GM12878	blood:	n/a	n/a
22	BCL3	chr10:43950641-43951526	A549	lung:	n/a	chr10:43951198-43951211
23	BCL3	chr10:43931947-43932506	A549	lung:	n/a	n/a
24	BCL3	chr10:43950596-43951564	A549	lung:	n/a	chr10:43951546-43951559 chr10:43951198-43951211
25	BCL3	chr10:43932077-43932543	GM12878	blood:	n/a	n/a
26	BCL3	chr10:43931842-43932588	A549	lung:	n/a	chr10:43932535-43932548
27	BCLAF1	chr10:43950713-43951657	GM12878	blood:	n/a	chr10:43951546-43951559 chr10:43951198-43951211
28	BCLAF1	chr10:43931700-43932534	GM12878	blood:	n/a	n/a
29	BCLAF1	chr10:43931644-43932564	GM12878	blood:	n/a	chr10:43932535-43932548
30	BCLAF1	chr10:43922623-43922985	GM12878	blood:	n/a	n/a
31	BCLAF1	chr10:43947203-43947836	GM12878	blood:	n/a	n/a
32	BCLAF1	chr10:43950763-43951532	GM12878	blood:	n/a	chr10:43951198-43951211
33	BHLHE40	chr10:43947344-43947944	GM12878	blood:	n/a	n/a
34	BHLHE40	chr10:43931800-43932646	K562	blood:	n/a	n/a
35	BHLHE40	chr10:43922968-43923180	K562	blood:	n/a	n/a
36	BHLHE40	chr10:43950747-43951492	K562	blood:	n/a	n/a
37	BHLHE40	chr10:43922640-43922989	GM12878	blood:	n/a	n/a
38	BHLHE40	chr10:43949083-43949174	K562	blood:	n/a	n/a
39	BHLHE40	chr10:43950751-43951668	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:43950727-43951484	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:43931955-43932635	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:43931754-43932600	HepG2	liver:	n/a	n/a
43	BRCA1	chr10:43931939-43932528	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr10:43931993-43932554	HepG2	liver:	n/a	n/a
45	BRCA1	chr10:43931883-43931903	GM12878	blood:	n/a	n/a
46	BRCA1	chr10:43950763-43951458	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr10:43950319-43951547	K562	blood:	n/a	n/a
48	CBX3	chr10:43950710-43951470	K562	blood:	n/a	n/a
49	CBX3	chr10:43930725-43931233	K562	blood:	n/a	n/a
50	CBX3	chr10:43931575-43933002	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43931089-43931139	ProgFib	skin:	n/a
2	chr10:43932900-43932950	HIPEpiC	eye:	n/a
3	chr10:43931089-43931139	ProgFib	skin:	n/a
4	chr10:43932900-43932950	HIPEpiC	eye:	n/a
5	chr10:43932466-43932516	HRCEpiC	kidney:	n/a
6	chr10:43932240-43932290	GM12878	blood:	n/a
7	chr10:43929290-43929340	PFSK-1	brain:	n/a
8	chr10:43931089-43931139	AG10803	skin:	n/a
9	chr10:43936838-43936888	ovcar-3	ovarian:	n/a
10	chr10:43932570-43932620	AG09309	skin:	n/a
11	chr10:43932570-43932620	Hepatocyte	liver:	n/a
12	chr10:43936838-43936888	RPTEC	kidney:	n/a
13	chr10:43942529-43942579	SKMC	muscle:	n/a
14	chr10:43947405-43947455	MCF-7	breast:	n/a
15	chr10:43936838-43936888	Hepatocyte	liver:	n/a
16	chr10:43929290-43929340	AG09309	skin:	n/a
17	chr10:43932466-43932516	BJ	skin:	n/a
18	chr10:43929290-43929340	HL-60	blood:	n/a
19	chr10:43932466-43932516	RPTEC	kidney:	n/a
20	chr10:43932449-43932499	NT2-D1	testis:	n/a
21	chr10:43932620-43932670	K562	blood:	n/a
22	chr10:43941753-43941803	NH-A	brain:	n/a
23	chr10:43936838-43936888	GM12891	blood:	n/a
24	chr10:43932620-43932670	AG04450	lung:	fetal
25	chr10:43932457-43932507	HRPEpiC	eye:	n/a
26	chr10:43932620-43932670	NB4	blood:	n/a
27	chr10:43936838-43936888	NB4	blood:	n/a
28	chr10:43932457-43932507	IMR90	lung:	fetal
29	chr10:43942529-43942579	AG04450	lung:	fetal
30	chr10:43932457-43932507	NB4	blood:	n/a
31	chr10:43950823-43950873	NHDF-neo	bronchial:	n/a
32	chr10:43931089-43931139	Hepatocyte	liver:	n/a
33	chr10:43947405-43947455	SKMC	muscle:	n/a
34	chr10:43932900-43932950	HRE	kidney:	n/a
35	chr10:43932457-43932507	HAEpiC	amniotic membrane:	n/a
36	chr10:43932570-43932620	SKMC	muscle:	n/a
37	chr10:43929290-43929340	HIPEpiC	eye:	n/a
38	chr10:43932466-43932516	HL-60	blood:	n/a
39	chr10:43932466-43932516	SKMC	muscle:	n/a
40	chr10:43931089-43931139	BE2_C	brain:	n/a
41	chr10:43932570-43932620	HCM	heart:	n/a
42	chr10:43929290-43929340	HCM	heart:	n/a
43	chr10:43932457-43932507	A549	lung:	n/a
44	chr10:43932457-43932507	HIPEpiC	eye:	n/a
45	chr10:43941753-43941803	PrEC	prostate:	n/a
46	chr10:43932620-43932670	SK-N-MC	brain:	n/a
47	chr10:43932466-43932516	PrEC	prostate:	n/a
48	chr10:43936838-43936888	CMK	blood:	n/a
49	chr10:43932900-43932950	GM12878	blood:	n/a
50	chr10:43932240-43932290	T-47D	breast:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:43919994..43922298-chr10:43925539..43927816,2	K562	blood:
2	chr10:43930579..43934633-chr10:43949587..43954210,8	K562	blood:
3	chr10:43943576..43945411-chr10:43948645..43950880,3	K562	blood:
4	chr10:43914769..43917445-chr10:43920064..43922045,2	MCF-7	breast:
5	chr10:43930452..43932223-chr17:43227607..43229368,2	K562	blood:
6	chr10:43890245..43893733-chr10:43950048..43952889,6	MCF-7	breast:
7	chr10:43950502..43951282-chr19:752665..753169,2	Hela-S3	cervix:
8	chr10:43930930..43934767-chr10:43936291..43939602,4	K562	blood:
9	chr10:43885901..43886431-chr10:43950839..43951795,3	MCF-7	breast:
10	chr10:43930912..43933891-chr10:43949765..43952473,2	MCF-7	breast:
11	chr10:43901381..43904812-chr10:43920194..43925203,8	MCF-7	breast:
12	chr10:43890830..43894030-chr10:43926925..43929713,4	MCF-7	breast:
13	chr10:43915403..43918859-chr10:43929644..43933431,7	K562	blood:
14	chr10:43912793..43917262-chr10:43929806..43934635,10	MCF-7	breast:
15	chr10:43943576..43945411-chr10:43948645..43950880,3	K562	blood:
16	chr10:43922499..43924905-chr10:43932128..43934196,2	MCF-7	breast:
17	chr10:43902513..43903341-chr10:43950698..43951343,2	HCT-116	colon:
18	chr10:43870160..43871851-chr10:43949319..43951127,2	K562	blood:
19	chr10:43931567..43932335-chr8:33342087..33342660,2	Hela-S3	cervix:
20	chr10:43926891..43929031-chr10:43930226..43934041,5	K562	blood:
21	chr10:43945671..43947485-chr10:43949391..43951784,2	K562	blood:
22	chr10:43932196..43932833-chr19:18433317..18434316,2	Hela-S3	cervix:
23	chr10:43929094..43930608-chr10:43936264..43939254,2	MCF-7	breast:
24	chr10:43941606..43943262-chr10:43948647..43951071,2	K562	blood:
25	chr10:43915062..43917461-chr10:43933933..43935575,2	MCF-7	breast:
26	chr10:43949801..43952727-chr10:43954596..43956488,2	K562	blood:
27	chr10:43932039..43932845-chr11:114166493..114167438,2	Hela-S3	cervix:
28	chr10:43903244..43904543-chr10:43931320..43932838,6	Hela-S3	cervix:
29	chr10:43914969..43916582-chr10:43923681..43926679,2	MCF-7	breast:
30	chr10:43931438..43934391-chr10:43934801..43937719,2	K562	blood:
31	chr10:43930579..43934633-chr10:43949587..43954210,8	K562	blood:
32	chr10:43929094..43930608-chr10:43936264..43939254,2	MCF-7	breast:
33	chr10:43943911..43945434-chr10:43948722..43951171,2	K562	blood:
34	chr10:43943009..43945472-chr10:43950940..43952726,2	MCF-7	breast:
35	chr10:43932225..43933767-chr10:43938510..43940620,2	MCF-7	breast:
36	chr10:43873108..43875014-chr10:43949897..43951449,2	MCF-7	breast:
37	chr10:43879008..43883052-chr10:43949060..43952010,4	K562	blood:
38	chr10:43931795..43932553-chr16:68271279..68271889,2	Hela-S3	cervix:
39	chr10:43889891..43893674-chr10:43930869..43934431,5	MCF-7	breast:
40	chr10:43901457..43906189-chr10:43948713..43953343,15	MCF-7	breast:
41	chr10:43843617..43844600-chr10:43950622..43951351,3	K562	blood:
42	chr1:45987496..45988124-chr10:43931979..43932884,2	Hela-S3	cervix:
43	chr10:43941606..43943262-chr10:43948647..43951071,2	K562	blood:
44	chr10:43931809..43932733-chr9:86594490..86595462,2	Hela-S3	cervix:
45	chr10:43856796..43859444-chr10:43950333..43952475,2	MCF-7	breast:
46	chr10:43919040..43921550-chr10:43937785..43940641,2	K562	blood:
47	chr10:43930874..43934590-chr10:43949528..43951985,5	K562	blood:
48	chr10:43913475..43914992-chr10:43935210..43936976,2	K562	blood:
49	chr10:43848475..43851407-chr10:43948589..43951104,3	MCF-7	breast:
50	chr10:43902184..43903883-chr10:43937396..43939761,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FXYD4-4	chr10:43932596-43932710	NONHSAT012968
2	lnc-ZNF487P-2	chr10:43927778-43928173	NONHSAT012966
3	lnc-ZNF487P-3	chr10:43926290-43927317	NONHSAT012965
4	lnc-FXYD4-4	chr10:43949513-43949980	NONHSAT012968
5	lnc-FXYD4-4	chr10:43947368-43950112	NONHSAT012969
6	lnc-FXYD4-4	chr10:43932574-43932710	NR_026693

No data

Variant related genes	Relation type
ZNF487	TF binding region
RNU7-193P	TF binding region
ZNF487	CpG island
RNU7-193P	CpG island
ENSG00000153406	chromatin interactions
ENSG00000198915	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000252532	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000221400	chromatin interactions
ENSG00000261469	chromatin interactions
ENSG00000166741	chromatin interactions
ENSG00000103415	chromatin interactions
ENSG00000243660	chromatin interactions
ENSG00000230555	chromatin interactions
ENSG00000198042	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000089597	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000158373	chromatin interactions

Extended variants
information (count: 1371 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1371 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150728039	chr10:43919996-43919997	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs55969732	chr10:43920009-43920010	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs116105828	chr10:43920025-43920026	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527791659	chr10:43920040-43920041	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs372933413	chr10:43920059-43920060	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs137882898	chr10:43920078-43920079	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs564554165	chr10:43920105-43920106	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191630663	chr10:43920106-43920107	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550486742	chr10:43920128-43920129	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184219760	chr10:43920129-43920130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369734482	chr10:43920163-43920164	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567664726	chr10:43920203-43920204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs71505675	chr10:43920242-43920243	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs71505676	chr10:43920245-43920246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372378237	chr10:43920272-43920273	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs60802454	chr10:43920273-43920274	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs56706302	chr10:43920283-43920284	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376986473	chr10:43920299-43920300	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548645784	chr10:43920302-43920303	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs60458319	chr10:43920303-43920304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548026432	chr10:43920304-43920305	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560256307	chr10:43920307-43920308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs59595614	chr10:43920308-43920309	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566532319	chr10:43920320-43920321	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs12249412	chr10:43920327-43920328	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375687074	chr10:43920377-43920378	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533876065	chr10:43920392-43920393	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs58461087	chr10:43920471-43920472	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570466623	chr10:43920502-43920503	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375350103	chr10:43920525-43920526	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs556447736	chr10:43920576-43920577	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113207977	chr10:43920577-43920578	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187408013	chr10:43920653-43920654	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577836689	chr10:43920678-43920679	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553556684	chr10:43920679-43920680	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs572206136	chr10:43920726-43920727	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545934695	chr10:43920728-43920729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564308618	chr10:43920745-43920746	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531760840	chr10:43920754-43920755	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547188925	chr10:43920757-43920758	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543474601	chr10:43920760-43920761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562372750	chr10:43920768-43920769	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529622779	chr10:43920782-43920783	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2819021	chr10:43920802-43920803	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115382853	chr10:43920804-43920805	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528960329	chr10:43920893-43920894	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527371209	chr10:43920901-43920902	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368730661	chr10:43920916-43920917	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2248335	chr10:43920941-43920942	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575349523	chr10:43920950-43920951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43916800-43920000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr10:43916800-43921200	Weak transcription	Primary T cells from cord blood	blood
3	chr10:43916800-43922400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr10:43916800-43931400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr10:43916800-43931600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:43916800-43931600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:43917000-43931600	Weak transcription	Fetal Brain Female	brain
8	chr10:43917200-43921200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr10:43917200-43921200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr10:43917200-43921200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr10:43917200-43921200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr10:43917200-43921400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr10:43917200-43921400	Weak transcription	GM12878-XiMat	blood
14	chr10:43917200-43921600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr10:43917200-43921600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:43917200-43922200	Weak transcription	Fetal Thymus	thymus
17	chr10:43917200-43922400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr10:43917200-43930800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:43917200-43930800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr10:43917200-43931600	Weak transcription	Brain Anterior Caudate	brain
21	chr10:43917400-43921200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr10:43917400-43921200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:43917400-43921200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:43917400-43921200	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:43917400-43921600	Weak transcription	Primary B cells from peripheral blood	blood
26	chr10:43917400-43922400	Weak transcription	Primary B cells from cord blood	blood
27	chr10:43917400-43930400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr10:43917400-43930800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr10:43917400-43930800	Weak transcription	Brain Hippocampus Middle	brain
30	chr10:43917400-43930800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr10:43917400-43930800	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr10:43917400-43931600	Weak transcription	Brain Angular Gyrus	brain
33	chr10:43917600-43921200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr10:43917600-43922000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr10:43917600-43922400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:43917600-43930800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:43917600-43930800	Weak transcription	Fetal Muscle Leg	muscle
38	chr10:43917600-43931600	Weak transcription	Right Ventricle	heart
39	chr10:43917800-43921400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr10:43918000-43928000	Weak transcription	Fetal Intestine Small	intestine
41	chr10:43918800-43920000	Enhancers	Liver	Liver
42	chr10:43919000-43920200	Enhancers	HepG2	liver
43	chr10:43919600-43920200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr10:43919800-43920000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr10:43919800-43920200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr10:43919800-43920200	Flanking Active TSS	Fetal Lung	lung
47	chr10:43919800-43926400	Weak transcription	K562	blood
48	chr10:43920000-43920200	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr10:43920000-43930400	Weak transcription	Liver	Liver
50	chr10:43920000-43930400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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