Variant report

Variant	esv2757996
Chromosome Location	chr5:61403138-61687817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3649)
CpG islands
(count:1223)
Chromatin interactive
region (count:214)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:3649 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61649868-61650221	K562	blood:	n/a	n/a
2	ARID3A	chr5:61604107-61605112	K562	blood:	n/a	n/a
3	ARID3A	chr5:61618221-61618789	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:61535193-61535231	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:61606306-61606906	K562	blood:	n/a	chr5:61606316-61606332 chr5:61606317-61606333
6	ARID3A	chr5:61687693-61687715	K562	blood:	n/a	n/a
7	ARID3A	chr5:61557348-61557786	K562	blood:	n/a	n/a
8	ARID3A	chr5:61636213-61636522	K562	blood:	n/a	n/a
9	ARID3A	chr5:61601596-61602035	K562	blood:	n/a	n/a
10	ARID3A	chr5:61581142-61581749	K562	blood:	n/a	n/a
11	ARID3A	chr5:61602387-61602432	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:61572650-61573748	K562	blood:	n/a	n/a
13	ARID3A	chr5:61616421-61616482	K562	blood:	n/a	n/a
14	ATF1	chr5:61572822-61573294	K562	blood:	n/a	n/a
15	ATF1	chr5:61495197-61495222	K562	blood:	n/a	n/a
16	ATF1	chr5:61496433-61496573	K562	blood:	n/a	n/a
17	ATF1	chr5:61548385-61548659	K562	blood:	n/a	n/a
18	ATF1	chr5:61531825-61531889	K562	blood:	n/a	n/a
19	ATF1	chr5:61671894-61672228	K562	blood:	n/a	n/a
20	ATF1	chr5:61601469-61601973	K562	blood:	n/a	n/a
21	ATF1	chr5:61602787-61603228	K562	blood:	n/a	n/a
22	ATF1	chr5:61639197-61639457	K562	blood:	n/a	n/a
23	ATF1	chr5:61529272-61529562	K562	blood:	n/a	n/a
24	ATF1	chr5:61611644-61612194	K562	blood:	n/a	n/a
25	ATF1	chr5:61557325-61557825	K562	blood:	n/a	n/a
26	ATF1	chr5:61615299-61615590	K562	blood:	n/a	n/a
27	ATF2	chr5:61581126-61581699	GM12878	blood:	n/a	n/a
28	ATF2	chr5:61601195-61601869	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr5:61602882-61603260	GM12878	blood:	n/a	n/a
30	ATF2	chr5:61585539-61586054	GM12878	blood:	n/a	n/a
31	ATF2	chr5:61552295-61552870	GM12878	blood:	n/a	n/a
32	ATF2	chr5:61602618-61603330	GM12878	blood:	n/a	n/a
33	ATF2	chr5:61552189-61552651	GM12878	blood:	n/a	n/a
34	ATF2	chr5:61581060-61581772	GM12878	blood:	n/a	n/a
35	ATF2	chr5:61601440-61601953	GM12878	blood:	n/a	n/a
36	ATF2	chr5:61601492-61602007	GM12878	blood:	n/a	n/a
37	ATF2	chr5:61572719-61573247	GM12878	blood:	n/a	n/a
38	ATF3	chr5:61529356-61529480	GM12878	blood:	n/a	n/a
39	ATF3	chr5:61623290-61623528	K562	blood:	n/a	n/a
40	ATF3	chr5:61601549-61601955	K562	blood:	n/a	n/a
41	BACH1	chr5:61581356-61581733	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr5:61573590-61573604	K562	blood:	n/a	n/a
43	BACH1	chr5:61601831-61602559	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr5:61562607-61562720	K562	blood:	n/a	n/a
45	BACH1	chr5:61557393-61557887	K562	blood:	n/a	n/a
46	BACH1	chr5:61602999-61603280	K562	blood:	n/a	n/a
47	BACH1	chr5:61671903-61672298	K562	blood:	n/a	chr5:61672102-61672116
48	BACH1	chr5:61681544-61681781	K562	blood:	n/a	n/a
49	BATF	chr5:61529263-61529683	GM12878	blood:	n/a	chr5:61529276-61529285 chr5:61529439-61529450 chr5:61529422-61529433
50	BATF	chr5:61585678-61585957	GM12878	blood:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61612144-61612194	Hela-S3	cervix:	n/a
2	chr5:61602737-61602787	HMEC	breast:	n/a
3	chr5:61602127-61602177	Hepatocyte	liver:	n/a
4	chr5:61612144-61612194	Hela-S3	cervix:	n/a
5	chr5:61602737-61602787	HMEC	breast:	n/a
6	chr5:61602127-61602177	Hepatocyte	liver:	n/a
7	chr5:61623163-61623213	RPTEC	kidney:	n/a
8	chr5:61420932-61420982	HCT-116	colon:	n/a
9	chr5:61433576-61433626	HUVEC	blood vessel:	n/a
10	chr5:61433576-61433626	ovcar-3	ovarian:	n/a
11	chr5:61439790-61439840	SK-N-MC	brain:	n/a
12	chr5:61612144-61612194	HCT-116	colon:	n/a
13	chr5:61601647-61601697	HCPEpiC	choroid plexus:	n/a
14	chr5:61433576-61433626	LNCaP	prostate:	n/a
15	chr5:61684420-61684470	BJ	skin:	n/a
16	chr5:61602737-61602787	HCM	heart:	n/a
17	chr5:61598126-61598176	GM19239	blood:	n/a
18	chr5:61602105-61602155	U87	brain:	n/a
19	chr5:61439790-61439840	PrEC	prostate:	n/a
20	chr5:61612144-61612194	PANC-1	pancreas:	n/a
21	chr5:61603122-61603172	K562	blood:	n/a
22	chr5:61420932-61420982	SK-N-SH_RA	brain:	n/a
23	chr5:61629825-61629875	Caco-2	colon:	n/a
24	chr5:61420932-61420982	Hela-S3	cervix:	n/a
25	chr5:61682030-61682080	GM06990	blood:	n/a
26	chr5:61602737-61602787	GM12892	blood:	n/a
27	chr5:61478616-61478666	HAEpiC	amniotic membrane:	n/a
28	chr5:61601128-61601178	GM19239	blood:	n/a
29	chr5:61601647-61601697	HRCEpiC	kidney:	n/a
30	chr5:61629825-61629875	NB4	blood:	n/a
31	chr5:61623163-61623213	ECC-1	luminal epithelium:	n/a
32	chr5:61598126-61598176	Jurkat	blood:	n/a
33	chr5:61605247-61605297	AG10803	skin:	n/a
34	chr5:61602737-61602787	K562	blood:	n/a
35	chr5:61601647-61601697	AG09319	gingival:	n/a
36	chr5:61433576-61433626	T-47D	breast:	n/a
37	chr5:61601529-61601579	H1-hESC	embryonic stem cell:	embryo
38	chr5:61601636-61601686	AG09319	gingival:	n/a
39	chr5:61684420-61684470	GM06990	blood:	n/a
40	chr5:61598126-61598176	HCM	heart:	n/a
41	chr5:61478616-61478666	RPTEC	kidney:	n/a
42	chr5:61601128-61601178	HNPCEpiC	eye:	n/a
43	chr5:61420932-61420982	RPTEC	kidney:	n/a
44	chr5:61684420-61684470	K562	blood:	n/a
45	chr5:61605247-61605297	ECC-1	luminal epithelium:	n/a
46	chr5:61603122-61603172	BJ	skin:	n/a
47	chr5:61433576-61433626	BJ	skin:	n/a
48	chr5:61601128-61601178	AG09309	skin:	n/a
49	chr5:61682030-61682080	HCPEpiC	choroid plexus:	n/a
50	chr5:61603122-61603172	SK-N-SH	brain:	n/a

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr5:61622771..61624897-chr5:61639078..61640701,2	K562	blood:
2	chr5:61622009..61624604-chr5:61628091..61630897,2	K562	blood:
3	chr5:61614359..61618770-chr5:61621420..61626796,7	K562	blood:
4	chr5:61558370..61559977-chr5:61580738..61582579,2	K562	blood:
5	chr5:61671360..61674176-chr5:61674605..61678360,3	MCF-7	breast:
6	chr5:61680086..61685494-chr5:61685831..61690801,7	MCF-7	breast:
7	chr5:61614359..61618770-chr5:61621420..61626796,7	K562	blood:
8	chr5:61570576..61576152-chr5:61577980..61582631,7	K562	blood:
9	chr5:61638389..61640483-chr5:61640496..61643629,3	K562	blood:
10	chr5:61574146..61576082-chr5:61601811..61603666,2	MCF-7	breast:
11	chr5:61576810..61579039-chr5:61601363..61604107,2	K562	blood:
12	chr5:61679991..61682016-chr5:61697548..61699312,2	MCF-7	breast:
13	chr5:61567482..61568420-chr5:61649640..61650468,3	MCF-7	breast:
14	chr5:61561179..61563178-chr5:61595838..61598010,2	K562	blood:
15	chr5:61675578..61677297-chr5:61689540..61692147,2	K562	blood:
16	chr5:61662871..61665721-chr5:61681464..61684214,2	K562	blood:
17	chr5:61614336..61618770-chr5:61621420..61625459,6	K562	blood:
18	chr5:61581288..61583777-chr5:61597562..61600246,2	K562	blood:
19	chr5:61602672..61603442-chr7:75544017..75544556,2	Hela-S3	cervix:
20	chr5:61550007..61554674-chr5:61558868..61565665,10	K562	blood:
21	chr5:61604944..61606842-chr5:61609048..61611891,3	MCF-7	breast:
22	chr5:61008135..61009057-chr5:61470844..61471443,2	K562	blood:
23	chr5:61580058..61581807-chr5:61582180..61584252,2	K562	blood:
24	chr5:61561395..61563266-chr5:61628626..61630582,2	K562	blood:
25	chr5:61555924..61558214-chr5:61579881..61582380,2	K562	blood:
26	chr5:61684677..61686970-chr5:61690927..61693209,3	K562	blood:
27	chr5:61561395..61563266-chr5:61628626..61630582,2	K562	blood:
28	chr5:61549033..61550848-chr5:61552778..61554762,2	K562	blood:
29	chr5:61604639..61607587-chr5:61647579..61650088,2	MCF-7	breast:
30	chr5:61439485..61439993-chr5:61501806..61502567,2	MCF-7	breast:
31	chr5:61471386..61473482-chr5:61474946..61477299,2	MCF-7	breast:
32	chr5:61562054..61563623-chr5:61613957..61616407,2	K562	blood:
33	chr5:61571856..61574619-chr5:61696505..61699367,2	K562	blood:
34	chr5:61507042..61508881-chr5:61509033..61511948,2	K562	blood:
35	chr5:61555834..61558737-chr5:61608990..61611037,2	MCF-7	breast:
36	chr5:61580058..61581807-chr5:61582180..61584252,2	K562	blood:
37	chr5:61593407..61596088-chr5:61596627..61599078,2	K562	blood:
38	chr5:61645558..61647477-chr5:61657497..61659462,2	K562	blood:
39	chr5:61643131..61645549-chr5:61650043..61651787,2	K562	blood:
40	chr5:61422681..61424219-chr5:61436524..61438145,2	MCF-7	breast:
41	chr5:61601612..61603523-chr5:61647478..61650855,3	MCF-7	breast:
42	chr5:61591991..61594374-chr5:61603392..61605599,2	K562	blood:
43	chr5:61554817..61557688-chr5:61629619..61631265,2	K562	blood:
44	chr5:61495766..61498313-chr5:61500945..61503625,2	MCF-7	breast:
45	chr5:61424317..61428011-chr5:61428590..61430862,3	K562	blood:
46	chr5:61471386..61473482-chr5:61474946..61477299,2	MCF-7	breast:
47	chr5:61686012..61687975-chr5:61698243..61700042,2	MCF-7	breast:
48	chr5:61501169..61503856-chr5:61511488..61513182,2	K562	blood:
49	chr5:61579949..61585428-chr5:61600379..61606921,7	K562	blood:
50	chr5:61653376..61655613-chr5:61657508..61659105,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF2A-2	chr5:61442492-61442773	NONHSAT101705

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KIF2A	hsa-miR-1	chr5:61681924-61681930
2	KIF2A	hsa-miR-183-5p	chr5:61682014-61682021
3	DIMT1L	hsa-miR-192-5p	chr5:61684806-61684826
4	KIF2A	hsa-miR-1	chr5:61681910-61681931
5	DIMT1L	hsa-miR-215-5p	chr5:61684806-61684826
6	KIF2A	hsa-miR-1	chr5:61682052-61682075
7	DIMT1L	hsa-miR-101-3p	chr5:61684519-61684539
8	KIF2A	hsa-miR-16-5p	chr5:61681397-61681413
9	KIF2A	hsa-miR-16-5p	chr5:61681406-61681413
10	KIF2A	hsa-miR-183-5p	chr5:61681997-61682021

Variant related genes	Relation type
DIMT1	TF binding region
KIF2A	TF binding region
RN7SKP157	TF binding region
DIMT1	CpG island
KIF2A	CpG island
RN7SKP157	CpG island
ENSG00000107864	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000251983	chromatin interactions
ENSG00000086189	chromatin interactions
ENSG00000086200	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000198060	chromatin interactions
ENSG00000068796	chromatin interactions
ENSG00000265345	chromatin interactions

Extended variants
information (count: 8448 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:8448 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557451855	chr5:61403154-61403155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559897259	chr5:61403171-61403172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147434406	chr5:61403194-61403195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181618538	chr5:61403195-61403196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116577190	chr5:61403240-61403241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541841011	chr5:61403285-61403286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531758455	chr5:61403293-61403294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185935414	chr5:61403310-61403311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571365533	chr5:61403337-61403338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534036430	chr5:61403427-61403428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114290042	chr5:61403462-61403463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139717841	chr5:61403464-61403465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560377881	chr5:61403473-61403474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535724867	chr5:61403566-61403567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142628167	chr5:61403627-61403628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372243864	chr5:61403628-61403629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150975257	chr5:61403674-61403675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4700472	chr5:61403681-61403682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs557995962	chr5:61403690-61403691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577622911	chr5:61403735-61403736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191348169	chr5:61403766-61403767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564571024	chr5:61403783-61403784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553710916	chr5:61403821-61403822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573582053	chr5:61403878-61403879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369874651	chr5:61403901-61403902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183270120	chr5:61403902-61403903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4700473	chr5:61403960-61403961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs374994778	chr5:61403963-61403964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537384062	chr5:61403977-61403978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531892502	chr5:61404040-61404041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545150486	chr5:61404067-61404068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565184702	chr5:61404188-61404189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527777679	chr5:61404211-61404212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186071865	chr5:61404266-61404267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200779621	chr5:61404315-61404316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567630504	chr5:61404372-61404373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190964464	chr5:61404374-61404375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550218025	chr5:61404409-61404410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182089647	chr5:61404427-61404428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558592948	chr5:61404445-61404446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149704815	chr5:61404455-61404456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187838729	chr5:61404561-61404562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549569689	chr5:61404570-61404571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192308451	chr5:61404611-61404612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2910468	chr5:61404673-61404674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs146692234	chr5:61404684-61404685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573692657	chr5:61404712-61404713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542175566	chr5:61404764-61404765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555742226	chr5:61404827-61404828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576325013	chr5:61404828-61404829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4144 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61398200-61409600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:61406800-61409000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:61407000-61409400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:61407000-61409400	Enhancers	Osteobl	bone
5	chr5:61407400-61408200	Enhancers	HSMM	muscle
6	chr5:61407800-61409200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:61407800-61409200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr5:61408000-61410000	Enhancers	HSMMtube	muscle
9	chr5:61408400-61409400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:61408600-61409000	Enhancers	Stomach Smooth Muscle	stomach
11	chr5:61409000-61409400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr5:61409200-61409400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
13	chr5:61409400-61411200	Enhancers	Stomach Smooth Muscle	stomach
14	chr5:61409600-61410400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:61410400-61410600	Enhancers	Fetal Stomach	stomach
16	chr5:61410400-61415800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:61416600-61417400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:61416600-61417600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:61417200-61417400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:61417200-61417600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:61417200-61417800	Enhancers	Esophagus	oesophagus
22	chr5:61417400-61417800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:61417800-61418000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr5:61418000-61418200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr5:61419800-61420200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:61419800-61420400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:61421400-61421800	Enhancers	NHEK	skin
28	chr5:61423000-61423400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:61424000-61424600	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr5:61424000-61424800	Enhancers	Brain Substantia Nigra	brain
31	chr5:61427200-61427400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:61427400-61428200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:61427600-61428800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:61427800-61428200	Enhancers	Osteobl	bone
35	chr5:61427800-61428400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:61427800-61428800	Enhancers	HMEC	breast
37	chr5:61427800-61429000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:61428000-61428400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:61428200-61429000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:61428200-61429200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:61428400-61428800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:61428800-61429000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:61428800-61430600	Weak transcription	HMEC	breast
44	chr5:61429000-61430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:61429200-61430200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:61430400-61430600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:61430400-61431000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:61430600-61431200	Enhancers	HMEC	breast
49	chr5:61430800-61431200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:61432400-61433200	Enhancers	HUES48 Cell Line	embryonic stem cell

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