Variant report

Variant	esv3338407
Chromosome Location	chr7:102714341-102716889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:855)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102715075-102715689	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102715479-102715490	K562	blood:	n/a	n/a
3	ATF2	chr7:102715018-102715634	GM12878	blood:	n/a	n/a
4	ATF3	chr7:102715170-102715696	K562	blood:	n/a	chr7:102715307-102715316
5	BACH1	chr7:102716301-102716459	K562	blood:	n/a	n/a
6	BACH1	chr7:102714777-102715487	K562	blood:	n/a	n/a
7	BACH1	chr7:102714954-102715637	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:102714922-102715397	A549	lung:	n/a	n/a
9	BCLAF1	chr7:102715413-102716333	GM12878	blood:	n/a	chr7:102716007-102716016 chr7:102716010-102716019 chr7:102716004-102716017 chr7:102716001-102716010 chr7:102715706-102715715 chr7:102715701-102715714
10	BHLHE40	chr7:102714705-102716143	GM12878	blood:	n/a	chr7:102715272-102715288
11	BHLHE40	chr7:102714627-102715752	K562	blood:	n/a	chr7:102715272-102715288
12	BHLHE40	chr7:102715088-102715737	HepG2	liver:	n/a	chr7:102715272-102715288
13	BRCA1	chr7:102715587-102715625	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr7:102715074-102715301	HepG2	liver:	n/a	n/a
15	BRCA1	chr7:102716098-102716377	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr7:102714725-102715413	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:102715205-102715586	GM12878	blood:	n/a	n/a
18	CBX3	chr7:102714539-102715680	K562	blood:	n/a	n/a
19	CCNT2	chr7:102714836-102715974	K562	blood:	n/a	chr7:102715307-102715316
20	CEBPB	chr7:102715045-102715539	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:102714951-102715703	MCF-7	breast:	n/a	n/a
22	CEBPB	chr7:102715005-102715625	A549	lung:	n/a	n/a
23	CEBPB	chr7:102714986-102715850	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:102715102-102715566	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:102715039-102715701	A549	lung:	n/a	n/a
26	CEBPB	chr7:102715038-102715630	K562	blood:	n/a	n/a
27	CEBPB	chr7:102714969-102715633	K562	blood:	n/a	n/a
28	CEBPB	chr7:102715133-102715600	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr7:102715168-102715570	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:102714788-102715680	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:102715268-102715408	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:102715249-102715521	K562	blood:	n/a	n/a
33	CEBPD	chr7:102715214-102715461	HepG2	liver:	n/a	n/a
34	CEBPD	chr7:102715034-102715817	K562	blood:	n/a	n/a
35	CEBPD	chr7:102715155-102716039	HepG2	liver:	n/a	n/a
36	CHD1	chr7:102715991-102716348	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr7:102716874-102716883	GM12878	blood:	n/a	n/a
38	CHD2	chr7:102716239-102716424	K562	blood:	n/a	n/a
39	CHD2	chr7:102716382-102716443	HepG2	liver:	n/a	n/a
40	CHD2	chr7:102714681-102715496	K562	blood:	n/a	n/a
41	CHD2	chr7:102714661-102716385	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr7:102715027-102715621	HepG2	liver:	n/a	n/a
43	CHD2	chr7:102714818-102716224	GM12878	blood:	n/a	n/a
44	CHD2	chr7:102714972-102715308	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:102714938-102715885	A549	lung:	n/a	n/a
46	CREB1	chr7:102714808-102716106	HepG2	liver:	n/a	n/a
47	CTCF	chr7:102715387-102715449	ProgFib	skin:	n/a	n/a
48	CTCF	chr7:102715320-102715470	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr7:102715200-102715350	HVMF	connective:	n/a	chr7:102715303-102715313 chr7:102715298-102715316
50	CTCF	chr7:102715280-102715430	HAc	cerebellar:	n/a	chr7:102715303-102715313 chr7:102715298-102715316

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102715559-102715609	HCPEpiC	choroid plexus:	n/a
2	chr7:102715559-102715609	HCPEpiC	choroid plexus:	n/a
3	chr7:102715209-102715259	NHDF-neo	bronchial:	n/a
4	chr7:102715559-102715609	AG04449	skin:	fetal
5	chr7:102715145-102715195	AG10803	skin:	n/a
6	chr7:102715191-102715241	Jurkat	blood:	n/a
7	chr7:102715565-102715615	K562	blood:	n/a
8	chr7:102715131-102715181	HNPCEpiC	eye:	n/a
9	chr7:102714871-102714921	NHDF-neo	bronchial:	n/a
10	chr7:102715145-102715195	HRCEpiC	kidney:	n/a
11	chr7:102715129-102715179	BJ	skin:	n/a
12	chr7:102716002-102716052	HCM	heart:	n/a
13	chr7:102715559-102715609	Hela-S3	cervix:	n/a
14	chr7:102715209-102715259	SKMC	muscle:	n/a
15	chr7:102715121-102715171	ECC-1	luminal epithelium:	n/a
16	chr7:102716072-102716122	AG04449	skin:	fetal
17	chr7:102715204-102715254	H1-hESC	embryonic stem cell:	embryo
18	chr7:102715121-102715171	HEEpiC	esophagus:	n/a
19	chr7:102715209-102715259	H1-hESC	embryonic stem cell:	embryo
20	chr7:102715204-102715254	GM12878	blood:	n/a
21	chr7:102715559-102715609	BJ	skin:	n/a
22	chr7:102715565-102715615	NB4	blood:	n/a
23	chr7:102715131-102715181	ovcar-3	ovarian:	n/a
24	chr7:102716002-102716052	AG04450	lung:	fetal
25	chr7:102715145-102715195	CMK	blood:	n/a
26	chr7:102715129-102715179	HepG2	liver:	n/a
27	chr7:102715131-102715181	SK-N-MC	brain:	n/a
28	chr7:102716072-102716122	HCT-116	colon:	n/a
29	chr7:102715232-102715282	AG04449	skin:	fetal
30	chr7:102715617-102715667	HEK293	kidney:	embryo
31	chr7:102714871-102714921	NT2-D1	testis:	n/a
32	chr7:102715209-102715259	Hepatocyte	liver:	n/a
33	chr7:102715191-102715241	HCPEpiC	choroid plexus:	n/a
34	chr7:102715204-102715254	PrEC	prostate:	n/a
35	chr7:102716072-102716122	T-47D	breast:	n/a
36	chr7:102715121-102715171	CMK	blood:	n/a
37	chr7:102715131-102715181	AG04450	lung:	fetal
38	chr7:102716002-102716052	ECC-1	luminal epithelium:	n/a
39	chr7:102715129-102715179	A549	lung:	n/a
40	chr7:102716072-102716122	GM12878	blood:	n/a
41	chr7:102715129-102715179	HIPEpiC	eye:	n/a
42	chr7:102714871-102714921	Caco-2	colon:	n/a
43	chr7:102715145-102715195	HAEpiC	amniotic membrane:	n/a
44	chr7:102715209-102715259	MCF-7	breast:	n/a
45	chr7:102715209-102715259	HAEpiC	amniotic membrane:	n/a
46	chr7:102715129-102715179	AG10803	skin:	n/a
47	chr7:102716072-102716122	GM06990	blood:	n/a
48	chr7:102716072-102716122	U87	brain:	n/a
49	chr7:102714871-102714921	AG09309	skin:	n/a
50	chr7:102715131-102715181	MCF-7	breast:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45987091..45988045-chr7:102714307..102715515,3	Hela-S3	cervix:
2	chr7:102714408..102716045-chr7:102987929..102989478,2	MCF-7	breast:
3	chr7:102714451..102716302-chr7:102729810..102731727,2	MCF-7	breast:
4	chr7:102388357..102390801-chr7:102713734..102717426,3	K562	blood:
5	chr7:102389494..102391981-chr7:102714130..102716680,2	MCF-7	breast:
6	chr7:102714022..102717631-chr7:102788669..102792237,6	MCF-7	breast:
7	chr7:102714987..102719162-chr7:102758108..102764327,6	K562	blood:
8	chr7:102713351..102719247-chr7:102725221..102729310,7	MCF-7	breast:
9	chr7:102713709..102715211-chr7:102789642..102791984,2	K562	blood:
10	chr7:102613006..102614516-chr7:102715583..102717366,2	K562	blood:
11	chr7:102714725..102717201-chr7:102788241..102791780,5	K562	blood:
12	chr7:102387955..102390990-chr7:102714406..102717094,4	MCF-7	breast:
13	chr22:20193823..20194749-chr7:102715063..102715854,2	HCT-116	colon:
14	chr7:102715561..102717346-chr7:102754713..102757374,2	MCF-7	breast:
15	chr7:102715186..102716960-chr7:102734053..102738564,5	K562	blood:
16	chr7:102714716..102718005-chr7:102734624..102737524,3	MCF-7	breast:
17	chr7:102715186..102716937-chr7:102734053..102736983,2	K562	blood:
18	chr3:156878407..156879008-chr7:102715174..102716014,2	Hela-S3	cervix:
19	chr7:102715629..102718160-chr7:102729461..102731149,2	K562	blood:
20	chr7:102714786..102716772-chr7:102789401..102791256,2	MCF-7	breast:
21	chr7:102714083..102716830-chr7:102726342..102727868,2	K562	blood:
22	chr17:56707584..56709248-chr7:102715096..102717010,2	MCF-7	breast:
23	chr7:102712172..102716042-chr7:102726342..102729326,4	K562	blood:
24	chr1:247495212..247495870-chr7:102715654..102716186,2	Hela-S3	cervix:
25	chr6:26154807..26157784-chr7:102714627..102716921,2	MCF-7	breast:
26	chr16:2014658..2015448-chr7:102714835..102715649,2	HCT-116	colon:
27	chr7:102715242..102717974-chr7:105515259..105517980,2	MCF-7	breast:
28	chr7:102715317..102716101-chrX:11775950..11776939,2	Hela-S3	cervix:
29	chr15:59225405..59226269-chr7:102715959..102716628,2	Hela-S3	cervix:
30	chr7:102714071..102718258-chr7:102757961..102760938,3	K562	blood:
31	chr7:102714740..102716868-chr7:102950642..102953182,2	MCF-7	breast:
32	chr20:53057077..53059223-chr7:102716078..102718486,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARMC10	TF binding region
FBXL13	TF binding region
ARMC10	CpG island
FBXL13	CpG island
ENSG00000105819	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000233025	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000235354	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000161057	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000005302	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000222011	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000236499	chromatin interactions
ENSG00000168298	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570723636	chr7:102714434-102714435	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs566615536	chr7:102714445-102714446	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs528594056	chr7:102714458-102714459	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs546363677	chr7:102714470-102714471	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs565294014	chr7:102714483-102714484	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs5886242	chr7:102714508-102714509	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs568262789	chr7:102714550-102714551	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs557576217	chr7:102714551-102714552	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs5886243	chr7:102714566-102714567	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs58939176	chr7:102714575-102714576	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11976834	chr7:102714638-102714639	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569103914	chr7:102714639-102714640	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs539431056	chr7:102714675-102714676	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs188132094	chr7:102714681-102714682	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs572952166	chr7:102714724-102714725	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs113806802	chr7:102714727-102714728	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs532677903	chr7:102714765-102714766	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs547570611	chr7:102714863-102714864	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs181319556	chr7:102714929-102714930	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs553254723	chr7:102714963-102714964	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs574984722	chr7:102714981-102714982	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs184006289	chr7:102715075-102715076	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs115390191	chr7:102715082-102715083	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs575570367	chr7:102715098-102715099	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs545772692	chr7:102715125-102715126	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs373871703	chr7:102715170-102715171	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
27	rs564163859	chr7:102715179-102715180	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs547035863	chr7:102715258-102715259	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
29	rs528532506	chr7:102715269-102715270	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
30	rs547082580	chr7:102715292-102715293	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
31	rs561686465	chr7:102715345-102715346	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
32	rs7797873	chr7:102715350-102715351	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550543139	chr7:102715351-102715352	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs563879411	chr7:102715358-102715359	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
35	rs569117550	chr7:102715387-102715388	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
36	rs539772233	chr7:102715394-102715395	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs551367320	chr7:102715414-102715415	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs566488462	chr7:102715425-102715426	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
39	rs533829468	chr7:102715448-102715449	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
40	rs7797786	chr7:102715457-102715458	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
41	rs11557627	chr7:102715461-102715462	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
42	rs565762426	chr7:102715465-102715466	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
43	rs116721018	chr7:102715471-102715472	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
44	rs536264677	chr7:102715545-102715546	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs575507046	chr7:102715572-102715573	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs546106574	chr7:102715584-102715585	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
47	rs564100581	chr7:102715610-102715611	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
48	rs111229327	chr7:102715618-102715619	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
49	rs562202783	chr7:102715626-102715627	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
50	rs529402253	chr7:102715630-102715631	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102702200-102714600	Weak transcription	Ovary	ovary
2	chr7:102710200-102714400	Weak transcription	Brain Angular Gyrus	brain
3	chr7:102711400-102714400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:102713400-102714400	Enhancers	Stomach Mucosa	stomach
5	chr7:102713800-102714400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:102713800-102714400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:102713800-102714400	Enhancers	Pancreas	Pancrea
8	chr7:102713800-102714600	Enhancers	Esophagus	oesophagus
9	chr7:102714000-102714400	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr7:102714000-102714400	Enhancers	Dnd41	blood
11	chr7:102714000-102716400	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr7:102714000-102716800	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr7:102714000-102717000	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr7:102714200-102714400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:102714200-102714400	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr7:102714200-102714400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:102714200-102714400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr7:102714200-102714400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:102714200-102714400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:102714200-102714400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr7:102714200-102714400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr7:102714200-102714400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:102714200-102714400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:102714200-102714400	Enhancers	Adipose Nuclei	Adipose
25	chr7:102714200-102714400	Enhancers	Liver	Liver
26	chr7:102714200-102714400	Enhancers	Brain Anterior Caudate	brain
27	chr7:102714200-102714400	Enhancers	Brain Cingulate Gyrus	brain
28	chr7:102714200-102714400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr7:102714200-102714400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr7:102714200-102714400	Enhancers	Brain Substantia Nigra	brain
31	chr7:102714200-102714400	Enhancers	Colonic Mucosa	Colon
32	chr7:102714200-102714400	Enhancers	Colon Smooth Muscle	Colon
33	chr7:102714200-102714400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr7:102714200-102714400	Enhancers	Fetal Intestine Large	intestine
35	chr7:102714200-102714400	Active TSS	Fetal Kidney	kidney
36	chr7:102714200-102714400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:102714200-102714400	Enhancers	Fetal Muscle Leg	muscle
38	chr7:102714200-102714400	Enhancers	Placenta	Placenta
39	chr7:102714200-102714400	Enhancers	Fetal Stomach	stomach
40	chr7:102714200-102714400	Enhancers	Placenta Amnion	Placenta Amnion
41	chr7:102714200-102714400	Enhancers	Rectal Smooth Muscle	rectum
42	chr7:102714200-102714400	Enhancers	Right Ventricle	heart
43	chr7:102714200-102714400	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr7:102714200-102714400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr7:102714200-102714400	Enhancers	Stomach Smooth Muscle	stomach
46	chr7:102714200-102714400	Enhancers	GM12878-XiMat	blood
47	chr7:102714200-102714400	Enhancers	HepG2	liver
48	chr7:102714200-102714400	Enhancers	HSMM	muscle
49	chr7:102714200-102714400	Enhancers	HSMMtube	muscle
50	chr7:102714200-102714400	Enhancers	Monocytes-CD14+_RO01746	blood

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