Variant report

Variant	nsv877650
Chromosome Location	chr3:151174010-151314449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:825)
CpG islands
(count:855)
Chromatin interactive
region (count:61)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:151222380-151222701	K562	blood:	n/a	n/a
2	ARID3A	chr3:151186194-151186396	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:151266023-151266248	K562	blood:	n/a	n/a
4	ATF1	chr3:151222400-151222729	K562	blood:	n/a	n/a
5	ATF1	chr3:151266012-151266321	K562	blood:	n/a	n/a
6	BACH1	chr3:151261357-151261724	K562	blood:	n/a	n/a
7	BACH1	chr3:151196217-151196234	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr3:151261413-151261613	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr3:151302504-151302757	GM12878	blood:	n/a	chr3:151302639-151302650
10	BATF	chr3:151302506-151302736	GM12878	blood:	n/a	chr3:151302639-151302650
11	BHLHE40	chr3:151222404-151222753	K562	blood:	n/a	n/a
12	BHLHE40	chr3:151298954-151299093	GM12878	blood:	n/a	n/a
13	CBX3	chr3:151265996-151266367	K562	blood:	n/a	n/a
14	CBX3	chr3:151222406-151222736	K562	blood:	n/a	n/a
15	CBX3	chr3:151305418-151305806	K562	blood:	n/a	n/a
16	CBX3	chr3:151200070-151200364	K562	blood:	n/a	n/a
17	CBX3	chr3:151193943-151194523	K562	blood:	n/a	n/a
18	CBX3	chr3:151222351-151222825	K562	blood:	n/a	n/a
19	CCNT2	chr3:151222451-151222775	K562	blood:	n/a	n/a
20	CEBPB	chr3:151194202-151194366	K562	blood:	n/a	n/a
21	CEBPB	chr3:151297807-151297972	K562	blood:	n/a	n/a
22	CEBPB	chr3:151297684-151298046	K562	blood:	n/a	n/a
23	CEBPB	chr3:151312087-151312178	K562	blood:	n/a	n/a
24	CEBPB	chr3:151180987-151181187	K562	blood:	n/a	n/a
25	CEBPB	chr3:151222371-151222708	K562	blood:	n/a	n/a
26	CEBPB	chr3:151265093-151265206	K562	blood:	n/a	n/a
27	CEBPB	chr3:151297739-151298032	K562	blood:	n/a	n/a
28	CEBPB	chr3:151265072-151265149	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:151271760-151272068	A549	lung:	n/a	chr3:151271884-151271895
30	CEBPB	chr3:151298985-151299057	K562	blood:	n/a	n/a
31	CEBPB	chr3:151261346-151261623	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:151275275-151275389	K562	blood:	n/a	chr3:151275345-151275356 chr3:151275346-151275357 chr3:151275345-151275358 chr3:151275345-151275358
33	CEBPB	chr3:151180990-151181277	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:151267735-151268313	MCF-7	breast:	n/a	chr3:151267981-151267994 chr3:151267983-151267994 chr3:151268116-151268129 chr3:151268117-151268128
35	CEBPB	chr3:151271723-151272013	H1-hESC	embryonic stem cell:	n/a	chr3:151271884-151271895
36	CEBPB	chr3:151271689-151272046	HepG2	liver:	n/a	chr3:151271884-151271895
37	CEBPB	chr3:151298477-151298699	A549	lung:	n/a	chr3:151298600-151298611 chr3:151298600-151298611 chr3:151298575-151298592
38	CEBPB	chr3:151271787-151271978	IMR90	lung:	n/a	chr3:151271884-151271895
39	CEBPB	chr3:151222510-151222703	K562	blood:	n/a	n/a
40	CEBPB	chr3:151309997-151310398	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:151298480-151298720	K562	blood:	n/a	chr3:151298600-151298611 chr3:151298600-151298611 chr3:151298575-151298592
42	CEBPB	chr3:151267964-151268143	A549	lung:	n/a	chr3:151267981-151267994 chr3:151267983-151267994 chr3:151268116-151268129 chr3:151268117-151268128
43	CEBPB	chr3:151271734-151271990	Hela-S3	cervix:	n/a	chr3:151271884-151271895
44	CEBPB	chr3:151271649-151272049	MCF-7	breast:	n/a	chr3:151271884-151271895
45	CEBPB	chr3:151298413-151298731	ECC-1	luminal epithelium:	n/a	chr3:151298600-151298611 chr3:151298600-151298611 chr3:151298575-151298592
46	CEBPB	chr3:151298386-151298792	Hela-S3	cervix:	n/a	chr3:151298600-151298611 chr3:151298600-151298611 chr3:151298575-151298592
47	CEBPB	chr3:151271701-151272038	K562	blood:	n/a	chr3:151271884-151271895
48	CEBPB	chr3:151267803-151268290	Hela-S3	cervix:	n/a	chr3:151267981-151267994 chr3:151267983-151267994 chr3:151268116-151268129 chr3:151268117-151268128
49	CEBPB	chr3:151298555-151298655	H1-hESC	embryonic stem cell:	n/a	chr3:151298600-151298611 chr3:151298600-151298611 chr3:151298575-151298592
50	CEBPB	chr3:151194138-151194434	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:151176600-151176650	ProgFib	skin:	n/a
2	chr3:151176600-151176650	ProgFib	skin:	n/a
3	chr3:151177285-151177335	NB4	blood:	n/a
4	chr3:151178727-151178777	AG04450	lung:	fetal
5	chr3:151178727-151178777	HRPEpiC	eye:	n/a
6	chr3:151178727-151178777	GM12891	blood:	n/a
7	chr3:151285666-151285716	NT2-D1	testis:	n/a
8	chr3:151177285-151177335	RPTEC	kidney:	n/a
9	chr3:151309377-151309427	GM12878	blood:	n/a
10	chr3:151177940-151177990	K562	blood:	n/a
11	chr3:151177285-151177335	SK-N-SH_RA	brain:	n/a
12	chr3:151309377-151309427	NHDF-neo	bronchial:	n/a
13	chr3:151176434-151176484	GM19239	blood:	n/a
14	chr3:151218968-151219018	HUVEC	blood vessel:	n/a
15	chr3:151309377-151309427	LNCaP	prostate:	n/a
16	chr3:151177940-151177990	HCPEpiC	choroid plexus:	n/a
17	chr3:151181976-151182026	GM19239	blood:	n/a
18	chr3:151177285-151177335	GM12878	blood:	n/a
19	chr3:151177285-151177335	ECC-1	luminal epithelium:	n/a
20	chr3:151218968-151219018	HMEC	breast:	n/a
21	chr3:151309377-151309427	SK-N-SH_RA	brain:	n/a
22	chr3:151178727-151178777	NHBE	bronchial:	n/a
23	chr3:151181976-151182026	Hepatocyte	liver:	n/a
24	chr3:151176684-151176734	AG10803	skin:	n/a
25	chr3:151178760-151178810	SAEC	small airway:	n/a
26	chr3:151176600-151176650	AG09309	skin:	n/a
27	chr3:151180389-151180439	HIPEpiC	eye:	n/a
28	chr3:151218968-151219018	HCPEpiC	choroid plexus:	n/a
29	chr3:151180389-151180439	HMEC	breast:	n/a
30	chr3:151177940-151177990	HRCEpiC	kidney:	n/a
31	chr3:151218968-151219018	MCF-7	breast:	n/a
32	chr3:151176684-151176734	HEEpiC	esophagus:	n/a
33	chr3:151285666-151285716	GM19239	blood:	n/a
34	chr3:151177940-151177990	HMEC	breast:	n/a
35	chr3:151309377-151309427	NHBE	bronchial:	n/a
36	chr3:151177940-151177990	HL-60	blood:	n/a
37	chr3:151309377-151309427	IMR90	lung:	fetal
38	chr3:151218968-151219018	CMK	blood:	n/a
39	chr3:151309377-151309427	T-47D	breast:	n/a
40	chr3:151178760-151178810	HNPCEpiC	eye:	n/a
41	chr3:151181976-151182026	HRPEpiC	eye:	n/a
42	chr3:151285666-151285716	HEEpiC	esophagus:	n/a
43	chr3:151178760-151178810	AoSMC	blood vessel:	n/a
44	chr3:151177285-151177335	SAEC	small airway:	n/a
45	chr3:151177940-151177990	AG10803	skin:	n/a
46	chr3:151180389-151180439	IMR90	lung:	fetal
47	chr3:151176600-151176650	NB4	blood:	n/a
48	chr3:151176434-151176484	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:151177940-151177990	PFSK-1	brain:	n/a
50	chr3:151178904-151178954	HEK293	kidney:	embryo

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:151194512..151197390-chr3:151199277..151201017,2	K562	blood:
2	chr3:151269368..151272288-chr3:151276113..151277874,2	K562	blood:
3	chr3:151259717..151261385-chr3:151267988..151270245,2	K562	blood:
4	chr3:151299413..151301641-chr3:151302443..151304307,2	K562	blood:
5	chr3:151267886..151269581-chr3:151272204..151274254,2	MCF-7	breast:
6	chr3:151301981..151304744-chr3:151305743..151307558,2	K562	blood:
7	chr3:151297378..151299096-chr3:151301123..151304068,3	K562	blood:
8	chr3:151259482..151261240-chr3:151262446..151265061,2	K562	blood:
9	chr3:151254596..151257098-chr3:151270755..151272685,2	K562	blood:
10	chr3:151299413..151301641-chr3:151302443..151304307,2	K562	blood:
11	chr3:151301981..151304744-chr3:151305743..151307558,2	K562	blood:
12	chr3:151254596..151257098-chr3:151270755..151272685,2	K562	blood:
13	chr3:151304607..151306547-chr3:151313096..151315639,2	K562	blood:
14	chr3:151176832..151178864-chr3:151180710..151183596,2	K562	blood:
15	chr3:151194378..151197390-chr3:151198956..151201017,3	K562	blood:
16	chr3:151238757..151241477-chr3:151264483..151267413,2	K562	blood:
17	chr3:151198937..151201376-chr3:151218846..151221278,2	K562	blood:
18	chr3:151255768..151257475-chr3:151274884..151276794,2	MCF-7	breast:
19	chr3:151267886..151269581-chr3:151272204..151274254,2	MCF-7	breast:
20	chr3:151255768..151257475-chr3:151274884..151276794,2	MCF-7	breast:
21	chr3:151189546..151191159-chr3:151195430..151197288,2	K562	blood:
22	chr3:151186067..151186742-chr3:151535761..151536727,2	MCF-7	breast:
23	chr3:151238757..151241477-chr3:151264483..151267413,2	K562	blood:
24	chr3:151171469..151173239-chr3:151178441..151180540,2	MCF-7	breast:
25	chr3:151253397..151255713-chr3:151264591..151266186,2	MCF-7	breast:
26	chr3:151194512..151197390-chr3:151199277..151201017,2	K562	blood:
27	chr3:151297378..151299096-chr3:151301123..151304068,3	K562	blood:
28	chr3:151258944..151262061-chr3:151269101..151271592,3	MCF-7	breast:
29	chr3:151303163..151304744-chr3:151305743..151307789,2	K562	blood:
30	chr3:151259482..151261240-chr3:151262446..151265061,2	K562	blood:
31	chr3:151224469..151226517-chr3:151258959..151260650,2	K562	blood:
32	chr3:151295351..151297607-chr3:151300115..151301880,2	K562	blood:
33	chr3:151220417..151222681-chr3:151461513..151463234,2	K562	blood:
34	chr3:151267449..151269580-chr3:151340230..151343017,2	K562	blood:
35	chr3:151252320..151254968-chr3:151257650..151259155,2	K562	blood:
36	chr3:151259717..151261385-chr3:151267988..151270245,2	K562	blood:
37	chr3:151252320..151254968-chr3:151257650..151259155,2	K562	blood:
38	chr3:151224469..151226517-chr3:151258959..151260650,2	K562	blood:
39	chr3:151253397..151255713-chr3:151264591..151266186,2	MCF-7	breast:
40	chr3:151255227..151257598-chr3:151259355..151262093,2	MCF-7	breast:
41	chr3:151296689..151298211-chr3:151300245..151302746,2	MCF-7	breast:
42	chr3:151219874..151221547-chr3:151223541..151225067,2	K562	blood:
43	chr3:151303163..151304744-chr3:151305743..151307789,2	K562	blood:
44	chr3:151198937..151201376-chr3:151218846..151221278,2	K562	blood:
45	chr3:151182500..151185282-chr3:151257399..151260037,2	K562	blood:
46	chr3:151295351..151297607-chr3:151300115..151301880,2	K562	blood:
47	chr3:151258944..151262061-chr3:151269101..151271592,3	MCF-7	breast:
48	chr3:151185862..151186560-chr3:151556517..151557100,2	MCF-7	breast:
49	chr3:151273045..151275315-chr3:151283671..151285920,2	K562	blood:
50	chr3:151182500..151185282-chr3:151257399..151260037,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IGSF10-3	chr3:151193592-151193962	NONHSAT092725
2	lnc-IGSF10-1	chr3:151299327-151299442	XLOC_003286
3	lnc-IGSF10-1	chr3:151256968-151257050	XLOC_003286
4	lnc-MED12L-3	chr3:151178589-151178685	l_2496_chr3:151171805-151178685_ovary

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5186	chr3:151283692-151283712	MIMAT0021116

No data

Variant related genes	Relation type
IGSF10	TF binding region
MIR5186	TF binding region
ENSG00000242119	TF binding region
MRPL42P6	TF binding region
IGSF10	CpG island
MIR5186	CpG island
ENSG00000242119	CpG island
MRPL42P6	CpG island
ENSG00000264330	chromatin interactions
ENSG00000152580	chromatin interactions

Extended variants
information (count: 5488 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5488 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2172248	chr3:151174010-151174011	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560056701	chr3:151174038-151174039	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117626279	chr3:151174069-151174070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532850947	chr3:151174123-151174124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139372646	chr3:151174157-151174158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73010422	chr3:151174165-151174166	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371920516	chr3:151174172-151174173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569284927	chr3:151174177-151174178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573105496	chr3:151174213-151174214	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190749130	chr3:151174219-151174220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555587447	chr3:151174220-151174221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371171945	chr3:151174308-151174309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565830865	chr3:151174368-151174369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534857276	chr3:151174482-151174483	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140592660	chr3:151174484-151174485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375250452	chr3:151174501-151174502	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527595156	chr3:151174524-151174525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552142537	chr3:151174533-151174534	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180828243	chr3:151174551-151174552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576463672	chr3:151174562-151174563	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531176715	chr3:151174568-151174569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542163625	chr3:151174658-151174659	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150465513	chr3:151174672-151174673	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549927089	chr3:151174704-151174705	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541648058	chr3:151174723-151174724	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368523900	chr3:151174724-151174725	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372250162	chr3:151174768-151174769	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549434122	chr3:151174772-151174773	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374156022	chr3:151174774-151174775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151292956	chr3:151174852-151174853	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376403738	chr3:151174896-151174897	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568155779	chr3:151174920-151174921	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138267408	chr3:151174967-151174968	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548690575	chr3:151175035-151175036	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536094667	chr3:151175149-151175150	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548018125	chr3:151175187-151175188	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565996843	chr3:151175208-151175209	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149284121	chr3:151175214-151175215	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184916390	chr3:151175229-151175230	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571430529	chr3:151175346-151175347	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539948883	chr3:151175363-151175364	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556648693	chr3:151175370-151175371	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576610111	chr3:151175371-151175372	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535884094	chr3:151175375-151175376	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555461938	chr3:151175376-151175377	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540146754	chr3:151175391-151175392	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541337923	chr3:151175395-151175396	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58354412	chr3:151175398-151175399	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577776620	chr3:151175408-151175409	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543603905	chr3:151175412-151175413	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	16773561	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151161600-151178600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:151168800-151178600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:151169000-151178400	Weak transcription	Aorta	Aorta
4	chr3:151171000-151176200	Weak transcription	Lung	lung
5	chr3:151171400-151177200	Weak transcription	Ovary	ovary
6	chr3:151171600-151174600	Weak transcription	Colon Smooth Muscle	Colon
7	chr3:151173200-151174800	Strong transcription	Fetal Lung	lung
8	chr3:151173800-151174400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr3:151173800-151176200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:151174400-151174600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:151174400-151177800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr3:151174600-151174800	Enhancers	Colon Smooth Muscle	Colon
13	chr3:151174600-151175400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:151174600-151178600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:151174800-151175600	Genic enhancers	Fetal Lung	lung
16	chr3:151174800-151176400	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:151175200-151175400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr3:151175400-151175600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:151175600-151176200	Weak transcription	Fetal Lung	lung
20	chr3:151175600-151176600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:151176200-151176400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr3:151176200-151176400	Active TSS	Fetal Lung	lung
23	chr3:151176200-151176400	Enhancers	Lung	lung
24	chr3:151176200-151177600	Enhancers	Fetal Stomach	stomach
25	chr3:151176400-151176600	Enhancers	Colon Smooth Muscle	Colon
26	chr3:151176400-151176600	Flanking Active TSS	Fetal Lung	lung
27	chr3:151176400-151178600	Weak transcription	Lung	lung
28	chr3:151176600-151176800	Enhancers	Fetal Lung	lung
29	chr3:151176600-151177000	Weak transcription	Colon Smooth Muscle	Colon
30	chr3:151176800-151177200	Active TSS	Fetal Lung	lung
31	chr3:151177000-151178200	Enhancers	Colon Smooth Muscle	Colon
32	chr3:151177200-151177400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr3:151177200-151177400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:151177200-151177600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
35	chr3:151177200-151177800	Enhancers	Ovary	ovary
36	chr3:151177200-151178200	Flanking Active TSS	Fetal Lung	lung
37	chr3:151177200-151178400	Active TSS	Adipose Nuclei	Adipose
38	chr3:151177200-151179200	Active TSS	Brain Hippocampus Middle	brain
39	chr3:151177200-151179200	Active TSS	Right Atrium	heart
40	chr3:151177400-151177800	Enhancers	Fetal Kidney	kidney
41	chr3:151177400-151178000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr3:151177400-151178400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:151177600-151177800	Active TSS	Dnd41	blood
44	chr3:151177600-151178400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:151177600-151178800	Active TSS	Stomach Smooth Muscle	stomach
46	chr3:151177800-151178000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr3:151177800-151178200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:151177800-151178200	Bivalent Enhancer	Fetal Kidney	kidney
49	chr3:151177800-151179200	Active TSS	Ovary	ovary
50	chr3:151177800-151179400	Flanking Active TSS	Dnd41	blood

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