Variant report

Variant	esv2752896
Chromosome Location	chr5:62073197-62846973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2503)
CpG islands
(count:369)
Chromatin interactive
region (count:68)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:62351150-62351392	K562	blood:	n/a	n/a
2	ATF1	chr5:62427553-62427829	K562	blood:	n/a	n/a
3	ATF1	chr5:62556872-62557055	K562	blood:	n/a	n/a
4	ATF1	chr5:62341251-62341425	K562	blood:	n/a	n/a
5	ATF1	chr5:62269440-62269840	K562	blood:	n/a	n/a
6	ATF1	chr5:62345801-62346021	K562	blood:	n/a	n/a
7	ATF2	chr5:62697361-62697668	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:62753304-62753329	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:62265689-62265873	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:62719905-62719946	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:62619812-62620109	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:62397553-62397673	K562	blood:	n/a	n/a
13	BACH1	chr5:62747193-62747244	K562	blood:	n/a	n/a
14	BACH1	chr5:62701318-62701374	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr5:62617005-62617179	GM12878	blood:	n/a	n/a
16	BCL3	chr5:62073699-62074050	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:62349021-62349249	HepG2	liver:	n/a	n/a
18	CBX3	chr5:62328193-62328706	K562	blood:	n/a	n/a
19	CBX3	chr5:62328196-62328627	K562	blood:	n/a	n/a
20	CEBPB	chr5:62257248-62257592	IMR90	lung:	n/a	chr5:62257416-62257427
21	CEBPB	chr5:62252472-62252672	A549	lung:	n/a	chr5:62252587-62252598 chr5:62252654-62252665
22	CEBPB	chr5:62251199-62251461	HepG2	liver:	n/a	chr5:62251358-62251369
23	CEBPB	chr5:62689106-62689423	HepG2	liver:	n/a	chr5:62689260-62689271
24	CEBPB	chr5:62257319-62257513	K562	blood:	n/a	chr5:62257416-62257427
25	CEBPB	chr5:62558040-62558371	A549	lung:	n/a	n/a
26	CEBPB	chr5:62659577-62659824	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:62497466-62498123	MCF-7	breast:	n/a	chr5:62497872-62497885
28	CEBPB	chr5:62183927-62184242	IMR90	lung:	n/a	chr5:62184085-62184096
29	CEBPB	chr5:62735865-62736193	IMR90	lung:	n/a	chr5:62736006-62736017
30	CEBPB	chr5:62279364-62279578	HepG2	liver:	n/a	chr5:62279489-62279500
31	CEBPB	chr5:62811699-62811898	HepG2	liver:	n/a	chr5:62811801-62811814
32	CEBPB	chr5:62086187-62086537	HepG2	liver:	n/a	chr5:62086349-62086360
33	CEBPB	chr5:62610605-62610681	A549	lung:	n/a	n/a
34	CEBPB	chr5:62839560-62839821	HepG2	liver:	n/a	chr5:62839727-62839738
35	CEBPB	chr5:62654328-62654539	HepG2	liver:	n/a	chr5:62654447-62654458
36	CEBPB	chr5:62558136-62558291	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:62654340-62654525	A549	lung:	n/a	chr5:62654447-62654458
38	CEBPB	chr5:62327101-62327449	HepG2	liver:	n/a	chr5:62327257-62327270 chr5:62327267-62327280 chr5:62327258-62327269 chr5:62327257-62327270
39	CEBPB	chr5:62257238-62257586	A549	lung:	n/a	chr5:62257416-62257427
40	CEBPB	chr5:62524047-62524356	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:62086167-62086547	HepG2	liver:	n/a	chr5:62086349-62086360
42	CEBPB	chr5:62606557-62606845	HepG2	liver:	n/a	chr5:62606691-62606702
43	CEBPB	chr5:62659595-62659835	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:62150450-62150720	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:62539757-62540049	MCF-7	breast:	n/a	chr5:62539843-62539854
46	CEBPB	chr5:62327148-62327448	IMR90	lung:	n/a	chr5:62327257-62327270 chr5:62327267-62327280 chr5:62327258-62327269 chr5:62327257-62327270
47	CEBPB	chr5:62086188-62086582	MCF-7	breast:	n/a	chr5:62086349-62086360
48	CEBPB	chr5:62086198-62086513	A549	lung:	n/a	chr5:62086349-62086360
49	CEBPB	chr5:62348904-62349222	HepG2	liver:	n/a	chr5:62349052-62349063 chr5:62349052-62349065
50	CEBPB	chr5:62252491-62252751	HepG2	liver:	n/a	chr5:62252587-62252598 chr5:62252654-62252665

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:62074572-62074622	HNPCEpiC	eye:	n/a
2	chr5:62073161-62073211	H1-hESC	embryonic stem cell:	embryo
3	chr5:62073161-62073211	ProgFib	skin:	n/a
4	chr5:62074572-62074622	HNPCEpiC	eye:	n/a
5	chr5:62073161-62073211	H1-hESC	embryonic stem cell:	embryo
6	chr5:62073161-62073211	ProgFib	skin:	n/a
7	chr5:62365115-62365165	HCM	heart:	n/a
8	chr5:62074261-62074311	HEEpiC	esophagus:	n/a
9	chr5:62100540-62100590	CMK	blood:	n/a
10	chr5:62100540-62100590	SK-N-SH_RA	brain:	n/a
11	chr5:62365115-62365165	SKMC	muscle:	n/a
12	chr5:62074572-62074622	HepG2	liver:	n/a
13	chr5:62100540-62100590	Hela-S3	cervix:	n/a
14	chr5:62073623-62073673	ProgFib	skin:	n/a
15	chr5:62074572-62074622	AG04450	lung:	fetal
16	chr5:62365115-62365165	HRE	kidney:	n/a
17	chr5:62074261-62074311	GM12891	blood:	n/a
18	chr5:62100540-62100590	HAEpiC	amniotic membrane:	n/a
19	chr5:62100540-62100590	PFSK-1	brain:	n/a
20	chr5:62073161-62073211	BE2_C	brain:	n/a
21	chr5:62073623-62073673	NHDF-neo	bronchial:	n/a
22	chr5:62074261-62074311	AG10803	skin:	n/a
23	chr5:62074572-62074622	ECC-1	luminal epithelium:	n/a
24	chr5:62074261-62074311	LNCaP	prostate:	n/a
25	chr5:62100540-62100590	HRE	kidney:	n/a
26	chr5:62073623-62073673	SAEC	small airway:	n/a
27	chr5:62365115-62365165	SK-N-SH	brain:	n/a
28	chr5:62073623-62073673	Caco-2	colon:	n/a
29	chr5:62074572-62074622	IMR90	lung:	fetal
30	chr5:62074261-62074311	ovcar-3	ovarian:	n/a
31	chr5:62073623-62073673	Hela-S3	cervix:	n/a
32	chr5:62073161-62073211	AG09309	skin:	n/a
33	chr5:62073623-62073673	SK-N-MC	brain:	n/a
34	chr5:62074572-62074622	HAEpiC	amniotic membrane:	n/a
35	chr5:62100540-62100590	BJ	skin:	n/a
36	chr5:62073623-62073673	HL-60	blood:	n/a
37	chr5:62074572-62074622	SK-N-MC	brain:	n/a
38	chr5:62073623-62073673	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:62073623-62073673	H1-hESC	embryonic stem cell:	embryo
40	chr5:62100540-62100590	AG09319	gingival:	n/a
41	chr5:62365115-62365165	NH-A	brain:	n/a
42	chr5:62074261-62074311	A549	lung:	n/a
43	chr5:62100540-62100590	AG04449	skin:	fetal
44	chr5:62073161-62073211	HUVEC	blood vessel:	n/a
45	chr5:62100540-62100590	GM06990	blood:	n/a
46	chr5:62073623-62073673	MCF10A-Er-Src	breast:	n/a
47	chr5:62073623-62073673	A549	lung:	n/a
48	chr5:62365115-62365165	ECC-1	luminal epithelium:	n/a
49	chr5:62074572-62074622	GM12878	blood:	n/a
50	chr5:62073623-62073673	HMEC	breast:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
2	chr5:62412476..62414687-chr5:62419094..62420921,2	K562	blood:
3	chr5:62697415..62698450-chr5:62724267..62725316,3	MCF-7	breast:
4	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
5	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
6	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
7	chr5:62697016..62697521-chr5:63907910..63908892,2	K562	blood:
8	chr17:56735253..56736865-chr5:62632692..62634192,4	K562	blood:
9	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
10	chr5:62503002..62504895-chr5:62506873..62508754,2	MCF-7	breast:
11	chr17:56736059..56737419-chr5:62632172..62633192,36	MCF-7	breast:
12	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
13	chr5:62421414..62422302-chr5:63258672..63259233,2	MCF-7	breast:
14	chr4:166297560..166298406-chr5:62742491..62743295,2	MCF-7	breast:
15	chr5:62582710..62584559-chr5:62585298..62587676,2	MCF-7	breast:
16	chr5:62688331..62691927-chr5:62694917..62699039,4	K562	blood:
17	chr5:62606697..62608384-chr5:62610156..62611740,2	MCF-7	breast:
18	chr5:62193925..62195577-chr5:62201485..62203661,2	MCF-7	breast:
19	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
20	chr5:62527630..62529181-chr5:62531232..62533377,2	MCF-7	breast:
21	chr5:62071591..62073108-chr5:62074194..62077077,2	K562	blood:
22	chr17:56735268..56738937-chr5:62632672..62634192,8	MCF-7	breast:
23	chr5:62272651..62274296-chr5:62275917..62277467,2	K562	blood:
24	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
25	chr2:239891948..239892626-chr5:62328345..62328845,2	K562	blood:
26	chr17:56736265..56737048-chr5:62632672..62633192,2	MCF-7	breast:
27	chr5:62193925..62195577-chr5:62201485..62203661,2	MCF-7	breast:
28	chr5:62697129..62697915-chr5:63258421..63259584,3	K562	blood:
29	chr5:62582710..62584559-chr5:62585298..62587676,2	MCF-7	breast:
30	chr5:62535956..62538795-chr5:62539410..62541239,2	K562	blood:
31	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
32	chr5:62542753..62544427-chr5:62547442..62548997,2	K562	blood:
33	chr5:62542467..62544427-chr5:62546236..62548997,2	K562	blood:
34	chr5:62681299..62684293-chr5:62685563..62687672,2	K562	blood:
35	chr5:62697027..62697873-chr5:63395970..63396618,2	MCF-7	breast:
36	chr17:56736170..56736865-chr5:62632672..62633192,4	Hela-S3	cervix:
37	chr5:62729811..62731369-chr5:62732550..62734446,2	MCF-7	breast:
38	chr5:62349615..62352403-chr5:62352864..62355347,2	MCF-7	breast:
39	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
40	chr5:62527630..62529181-chr5:62531232..62533377,2	MCF-7	breast:
41	chr5:62421372..62422126-chr5:63259016..63259610,3	MCF-7	breast:
42	chr5:62744743..62747073-chr5:62749692..62752090,2	K562	blood:
43	chr17:56736153..56736969-chr5:62632172..62633192,8	HCT-116	colon:
44	chr5:62421535..62422320-chr5:62693970..62694916,3	MCF-7	breast:
45	chr17:56734221..56737941-chr5:62631172..62634192,18	MCF-7	breast:
46	chr5:62349615..62352403-chr5:62352864..62355347,2	MCF-7	breast:
47	chr17:56736164..56737083-chr5:62632172..62633192,29	MCF-7	breast:
48	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
49	chr5:62730491..62733268-chr5:62735229..62737200,2	K562	blood:
50	chr5:62272651..62274296-chr5:62275917..62277467,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIMT1-5	chr5:62318746-62319316	NONHSAT101720

No data

Variant related genes	Relation type
ISCA1P1	TF binding region
ENSG00000248185	TF binding region
ENSG00000249579	TF binding region
ISCA1P1	CpG island
ENSG00000248185	CpG island
ENSG00000249579	CpG island
ENSG00000217416	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 10175 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:10175 , 50 per page) page: 1 2 3 4 5 6 7 ... 204

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16891065	chr5:62073197-62073198	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554406238	chr5:62073629-62073630	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs568198560	chr5:62073641-62073642	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs568228035	chr5:62073644-62073645	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs558455672	chr5:62073702-62073703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536598595	chr5:62073733-62073734	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs78854674	chr5:62073765-62073766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs545380607	chr5:62073767-62073768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs376646992	chr5:62073771-62073772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2591790	chr5:62073783-62073784	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs139788896	chr5:62073784-62073785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs386688525	chr5:62073792-62073793	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2642779	chr5:62073794-62073795	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs112586905	chr5:62073800-62073801	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542602889	chr5:62073804-62073805	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563607470	chr5:62073813-62073814	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2642780	chr5:62073834-62073835	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs367978998	chr5:62073863-62073864	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs181286872	chr5:62073877-62073878	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558911778	chr5:62073882-62073883	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs573439142	chr5:62073929-62073930	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540857753	chr5:62073974-62073975	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs528106684	chr5:62073980-62073981	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568935672	chr5:62073981-62073982	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs185572720	chr5:62073983-62073984	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs537214433	chr5:62073984-62073985	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139436964	chr5:62074215-62074216	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57512050	chr5:62074218-62074219	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs398064857	chr5:62074232-62074233	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565306494	chr5:62074247-62074248	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs58178498	chr5:62074248-62074249	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs6899144	chr5:62074272-62074273	Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539742190	chr5:62074301-62074302	Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs140678680	chr5:62074305-62074306	Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188371870	chr5:62074345-62074346	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs180789694	chr5:62074409-62074410	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555021133	chr5:62074413-62074414	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201853744	chr5:62074434-62074435	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574853649	chr5:62074455-62074456	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146491061	chr5:62074488-62074489	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543560751	chr5:62074500-62074501	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs16891072	chr5:62074510-62074511	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs535204292	chr5:62074515-62074516	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577072710	chr5:62074554-62074555	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546068064	chr5:62074617-62074618	Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs16891075	chr5:62074697-62074698	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs16891077	chr5:62074718-62074719	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
48	rs547900284	chr5:62074735-62074736	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs115455050	chr5:62074737-62074738	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530529561	chr5:62074787-62074788	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:62073800-62074000	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr5:62073800-62074600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:62074000-62074200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr5:62074000-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:62074000-62075000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr5:62074000-62075400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:62074200-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:62074200-62074800	Enhancers	Fetal Lung	lung
9	chr5:62074200-62075000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr5:62074200-62075000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr5:62074400-62074600	Enhancers	Primary hematopoietic stem cells	blood
12	chr5:62074400-62075000	Enhancers	Primary B cells from cord blood	blood
13	chr5:62074400-62075000	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr5:62074400-62075400	Enhancers	Fetal Kidney	kidney
15	chr5:62074600-62074800	Flanking Active TSS	Primary hematopoietic stem cells	blood
16	chr5:62074600-62075000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
17	chr5:62074600-62075000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr5:62074600-62075000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:62074600-62075000	Enhancers	Dnd41	blood
20	chr5:62074800-62075000	Active TSS	Primary hematopoietic stem cells	blood
21	chr5:62074800-62075000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr5:62074800-62075000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr5:62074800-62075400	Enhancers	Brain Hippocampus Middle	brain
24	chr5:62075000-62077800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr5:62075000-62079000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr5:62075000-62079200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:62075000-62079200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr5:62076200-62076800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:62076200-62077000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr5:62077800-62078200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr5:62078200-62079200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr5:62078800-62079400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:62078800-62079600	Enhancers	GM12878-XiMat	blood
34	chr5:62079000-62079600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr5:62079200-62079400	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr5:62079200-62079400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:62079200-62079600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr5:62079400-62079600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:62079600-62079800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:62083800-62084000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:62084000-62086400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:62086000-62086800	Enhancers	Liver	Liver
43	chr5:62086200-62087000	Enhancers	Ovary	ovary
44	chr5:62100200-62100800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:62100200-62101000	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr5:62100200-62101200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:62100200-62101400	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr5:62100400-62100800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr5:62100400-62100800	Active TSS	H1 Cell Line	embryonic stem cell
50	chr5:62100400-62100800	Active TSS	H9 Cell Line	embryonic stem cell

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