Variant report

Variant	esv1819303
Chromosome Location	chr6:150093678-150132092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:142)
CpG islands
(count:61)
Chromatin interactive
region (count:35)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:142 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr6:150100819-150100990	GM12878	blood:	n/a	n/a
2	BHLHE40	chr6:150116979-150117158	K562	blood:	n/a	chr6:150117065-150117086 chr6:150117070-150117079
3	CCNT2	chr6:150095023-150095118	K562	blood:	n/a	n/a
4	CEBPB	chr6:150098433-150098649	IMR90	lung:	n/a	n/a
5	CEBPB	chr6:150102851-150103107	K562	blood:	n/a	chr6:150102954-150102965
6	CEBPB	chr6:150106213-150106402	K562	blood:	n/a	n/a
7	CEBPB	chr6:150102801-150103114	HepG2	liver:	n/a	chr6:150102954-150102965
8	CEBPB	chr6:150128928-150129144	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:150102851-150103103	IMR90	lung:	n/a	chr6:150102954-150102965
10	CTCF	chr6:150129862-150129921	GM20000	blood:	n/a	n/a
11	CTCF	chr6:150131080-150131230	Caco-2	colon:	n/a	n/a
12	CTCF	chr6:150123285-150123592	T-47D	breast:	n/a	n/a
13	CTCF	chr6:150099418-150099462	Lung_OC	lung:	n/a	n/a
14	CTCF	chr6:150119065-150119161	Lung_OC	lung:	n/a	n/a
15	CTCF	chr6:150115785-150115848	Kidney_OC	kidney:	n/a	n/a
16	EBF1	chr6:150112228-150112457	GM12878	blood:	n/a	chr6:150112332-150112341 chr6:150112330-150112343 chr6:150112332-150112342
17	ELF1	chr6:150127356-150127612	K562	blood:	n/a	n/a
18	ELF1	chr6:150127291-150127599	K562	blood:	n/a	n/a
19	EP300	chr6:150111030-150111045	GM12878	blood:	n/a	n/a
20	FOXA2	chr6:150114116-150114316	A549	lung:	n/a	n/a
21	GATA1	chr6:150126173-150126447	PBDE	blood:	n/a	n/a
22	GATA3	chr6:150110877-150111207	MCF-7	breast:	n/a	n/a
23	GATA3	chr6:150110906-150111113	MCF-7	breast:	n/a	n/a
24	GATA3	chr6:150110939-150111116	SH-SY5Y	brain:	n/a	n/a
25	GTF2F1	chr6:150129567-150129579	H1-hESC	embryonic stem cell:	n/a	n/a
26	IRF1	chr6:150103335-150103555	K562	blood:	n/a	n/a
27	JUND	chr6:150101428-150101459	K562	blood:	n/a	n/a
28	MAFK	chr6:150105148-150105183	K562	blood:	n/a	n/a
29	NR2F2	chr6:150106569-150106940	K562	blood:	n/a	n/a
30	NR2F2	chr6:150106550-150107026	K562	blood:	n/a	n/a
31	NRF1	chr6:150131183-150131273	GM12878	blood:	n/a	n/a
32	POLR2A	chr6:150118529-150118704	K562	blood:	n/a	n/a
33	POLR2A	chr6:150112420-150113125	K562	blood:	n/a	n/a
34	POLR2A	chr6:150119194-150119261	Gliobla	brain:	n/a	n/a
35	POLR2A	chr6:150115732-150116033	K562	blood:	n/a	n/a
36	POLR2A	chr6:150127266-150127621	MCF-7	breast:	n/a	n/a
37	POLR2A	chr6:150129036-150129624	K562	blood:	n/a	n/a
38	POLR2A	chr6:150098222-150098279	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr6:150124248-150126737	K562	blood:	n/a	n/a
40	POLR2A	chr6:150112069-150112115	K562	blood:	n/a	n/a
41	POLR2A	chr6:150115710-150116049	K562	blood:	n/a	n/a
42	POLR2A	chr6:150094639-150094780	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr6:150127744-150127885	MCF-7	breast:	n/a	n/a
44	POLR2A	chr6:150124187-150124752	K562	blood:	n/a	n/a
45	POLR2A	chr6:150122916-150123029	K562	blood:	n/a	n/a
46	POLR2A	chr6:150127643-150127645	MCF-7	breast:	n/a	n/a
47	POLR2A	chr6:150113776-150113809	K562	blood:	n/a	n/a
48	POLR2A	chr6:150096573-150096728	K562	blood:	n/a	n/a
49	POLR2A	chr6:150100281-150100339	ProgFib	skin:	n/a	n/a
50	POLR2A	chr6:150126268-150126358	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150128134-150128184	HCF	heart:	n/a
2	chr6:150128134-150128184	HAEpiC	amniotic membrane:	n/a
3	chr6:150128134-150128184	NHDF-neo	bronchial:	n/a
4	chr6:150128134-150128184	BJ	skin:	n/a
5	chr6:150128134-150128184	LNCaP	prostate:	n/a
6	chr6:150128134-150128184	HL-60	blood:	n/a
7	chr6:150128134-150128184	BE2_C	brain:	n/a
8	chr6:150128134-150128184	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:150128134-150128184	CMK	blood:	n/a
10	chr6:150128134-150128184	K562	blood:	n/a
11	chr6:150128134-150128184	A549	lung:	n/a
12	chr6:150128134-150128184	HepG2	liver:	n/a
13	chr6:150128134-150128184	AG09309	skin:	n/a
14	chr6:150128134-150128184	HRE	kidney:	n/a
15	chr6:150128134-150128184	HEEpiC	esophagus:	n/a
16	chr6:150128134-150128184	NT2-D1	testis:	n/a
17	chr6:150128134-150128184	HNPCEpiC	eye:	n/a
18	chr6:150128134-150128184	Hela-S3	cervix:	n/a
19	chr6:150128134-150128184	SKMC	muscle:	n/a
20	chr6:150128134-150128184	Hepatocyte	liver:	n/a
21	chr6:150128134-150128184	HRPEpiC	eye:	n/a
22	chr6:150128134-150128184	HMEC	breast:	n/a
23	chr6:150128134-150128184	HIPEpiC	eye:	n/a
24	chr6:150128134-150128184	RPTEC	kidney:	n/a
25	chr6:150128134-150128184	HCPEpiC	choroid plexus:	n/a
26	chr6:150128134-150128184	H1-hESC	embryonic stem cell:	embryo
27	chr6:150128134-150128184	SK-N-SH	brain:	n/a
28	chr6:150128134-150128184	NB4	blood:	n/a
29	chr6:150128134-150128184	MCF-7	breast:	n/a
30	chr6:150128134-150128184	AG04449	skin:	fetal
31	chr6:150128134-150128184	SAEC	small airway:	n/a
32	chr6:150128134-150128184	GM19239	blood:	n/a
33	chr6:150128134-150128184	ProgFib	skin:	n/a
34	chr6:150128134-150128184	T-47D	breast:	n/a
35	chr6:150128134-150128184	HCM	heart:	n/a
36	chr6:150128134-150128184	ovcar-3	ovarian:	n/a
37	chr6:150128134-150128184	AG10803	skin:	n/a
38	chr6:150128134-150128184	GM12892	blood:	n/a
39	chr6:150128134-150128184	AoSMC	blood vessel:	n/a
40	chr6:150128134-150128184	U87	brain:	n/a
41	chr6:150128134-150128184	NH-A	brain:	n/a
42	chr6:150128134-150128184	PANC-1	pancreas:	n/a
43	chr6:150128134-150128184	NHBE	bronchial:	n/a
44	chr6:150128134-150128184	GM12878	blood:	n/a
45	chr6:150128134-150128184	Caco-2	colon:	n/a
46	chr6:150128134-150128184	SK-N-SH_RA	brain:	n/a
47	chr6:150128134-150128184	AG04450	lung:	fetal
48	chr6:150128134-150128184	PrEC	prostate:	n/a
49	chr6:150128134-150128184	PFSK-1	brain:	n/a
50	chr6:150128134-150128184	SK-N-MC	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150069126..150071489-chr6:150107300..150111812,4	K562	blood:
2	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
3	chr6:150070320..150072055-chr6:150100262..150102859,2	K562	blood:
4	chr6:150075712..150077814-chr6:150098516..150101508,2	K562	blood:
5	chr6:150116018..150118922-chr6:150120645..150124683,3	K562	blood:
6	chr6:150123377..150125799-chr6:150184381..150186208,2	MCF-7	breast:
7	chr6:150127349..150128879-chr6:150131415..150134215,2	K562	blood:
8	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
9	chr6:150120002..150121687-chr6:150123365..150125710,2	K562	blood:
10	chr6:150103039..150105538-chr6:150109602..150113560,4	K562	blood:
11	chr6:150067696..150070482-chr6:150117638..150119336,2	K562	blood:
12	chr6:150055968..150058286-chr6:150092691..150095282,2	K562	blood:
13	chr6:150120002..150121687-chr6:150123365..150125710,2	K562	blood:
14	chr6:150037962..150039498-chr6:150131610..150134476,2	K562	blood:
15	chr6:150103039..150105538-chr6:150109602..150113560,4	K562	blood:
16	chr6:150127349..150128879-chr6:150131415..150134215,2	K562	blood:
17	chr1:16160895..16163789-chr6:150103318..150105332,2	K562	blood:
18	chr6:150073818..150075342-chr6:150092909..150094549,2	K562	blood:
19	chr6:150103186..150105713-chr6:150110065..150112313,2	MCF-7	breast:
20	chr6:150127289..150128879-chr6:150131415..150134275,2	K562	blood:
21	chr6:150066753..150069159-chr6:150105236..150106762,2	K562	blood:
22	chr6:150068365..150071134-chr6:150101769..150103680,2	K562	blood:
23	chr6:150116018..150118922-chr6:150120645..150124683,3	K562	blood:
24	chr6:150127289..150128879-chr6:150131415..150134275,2	K562	blood:
25	chr6:150069972..150072484-chr6:150117277..150119937,2	MCF-7	breast:
26	chr6:150103684..150106554-chr6:150183972..150185592,2	MCF-7	breast:
27	chr6:150088901..150091246-chr6:150095391..150098115,2	MCF-7	breast:
28	chr6:150115210..150117160-chr6:150126668..150131060,3	MCF-7	breast:
29	chr6:150075319..150077363-chr6:150091174..150093691,2	MCF-7	breast:
30	chr6:150092888..150094576-chr6:150096247..150098891,2	K562	blood:
31	chr6:150103186..150105713-chr6:150110065..150112313,2	MCF-7	breast:
32	chr6:150092888..150094576-chr6:150096247..150098891,2	K562	blood:
33	chr6:150069990..150071882-chr6:150109798..150112486,2	MCF-7	breast:
34	chr6:150085048..150087027-chr6:150091947..150093777,2	MCF-7	breast:
35	chr6:150068651..150072384-chr6:150088938..150093926,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP2-6	chr6:150131176-150131259	NONHSAT115511
2	lnc-LRP11-1	chr6:150117711-150118575	ENSG00000231760.2
3	lnc-ULBP2-6	chr6:150131752-150132044	NONHSAT115511
4	lnc-LRP11-1	chr6:150118392-150118575	ENSG00000231760.1
5	lnc-LRP11-1	chr6:150119057-150119308	ENSG00000231760.2
6	lnc-LRP11-1	chr6:150119057-150119308	ENSG00000231760.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PCMT1	hsa-miR-16-5p	chr6:150124321-150124327

Variant related genes	Relation type
PCMT1	TF binding region
ENSG00000219433	TF binding region
ENSG00000231760	TF binding region
PCMT1	CpG island
ENSG00000219433	CpG island
ENSG00000231760	CpG island
ENSG00000179743	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000268592	chromatin interactions
ENSG00000120265	chromatin interactions
ENSG00000219433	chromatin interactions
ENSG00000131023	chromatin interactions

Extended variants
information (count: 1569 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1569 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3805748	chr6:150093678-150093679	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3805749	chr6:150093682-150093683	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs542496441	chr6:150093701-150093702	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs558170673	chr6:150093744-150093745	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553589844	chr6:150093812-150093813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567202075	chr6:150093875-150093876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147577776	chr6:150093891-150093892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs140298308	chr6:150093892-150093893	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555994803	chr6:150093919-150093920	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575144197	chr6:150093925-150093926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11155681	chr6:150093968-150093969	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs11155682	chr6:150093981-150093982	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs551133684	chr6:150093988-150093989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531926929	chr6:150094013-150094014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149213514	chr6:150094014-150094015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559935591	chr6:150094036-150094037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529057717	chr6:150094043-150094044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542560956	chr6:150094046-150094047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570965197	chr6:150094070-150094071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562761352	chr6:150094084-150094085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376128127	chr6:150094085-150094086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9397301	chr6:150094087-150094088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533417307	chr6:150094110-150094111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373290909	chr6:150094152-150094153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533583667	chr6:150094153-150094154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550990742	chr6:150094170-150094171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377327204	chr6:150094172-150094173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570985481	chr6:150094178-150094179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533448171	chr6:150094191-150094192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376494621	chr6:150094227-150094228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372113772	chr6:150094241-150094242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192061519	chr6:150094253-150094254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143477308	chr6:150094288-150094289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78000187	chr6:150094344-150094345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78734936	chr6:150094345-150094346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567089019	chr6:150094359-150094360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113346306	chr6:150094418-150094419	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs548443885	chr6:150094470-150094471	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs71709110	chr6:150094487-150094488	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs377225556	chr6:150094512-150094513	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs75260901	chr6:150094534-150094535	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs11961451	chr6:150094546-150094547	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs151299021	chr6:150094553-150094554	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs186480410	chr6:150094557-150094558	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs189714682	chr6:150094590-150094591	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs140518958	chr6:150094607-150094608	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs553405327	chr6:150094614-150094615	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs368679571	chr6:150094637-150094638	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs9765965	chr6:150094655-150094656	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs542797526	chr6:150094690-150094691	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150071800-150100200	Weak transcription	Gastric	stomach
2	chr6:150072000-150094200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:150072000-150111000	Weak transcription	Fetal Kidney	kidney
4	chr6:150072000-150152000	Weak transcription	Aorta	Aorta
5	chr6:150072400-150104600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr6:150072400-150111400	Weak transcription	Colonic Mucosa	Colon
7	chr6:150073000-150094400	Weak transcription	Lung	lung
8	chr6:150073800-150182400	Weak transcription	Fetal Brain Male	brain
9	chr6:150074200-150101000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:150075800-150094800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr6:150077000-150115400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:150077200-150118400	Weak transcription	Pancreas	Pancrea
13	chr6:150077400-150142400	Weak transcription	Fetal Heart	heart
14	chr6:150077800-150118400	Weak transcription	Psoas Muscle	Psoas
15	chr6:150081600-150101200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:150087000-150093800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:150087000-150096600	Weak transcription	Esophagus	oesophagus
18	chr6:150087200-150095400	Strong transcription	Primary T cells from cord blood	blood
19	chr6:150087200-150154000	Weak transcription	Small Intestine	intestine
20	chr6:150087400-150134000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:150087600-150117400	Weak transcription	Brain Substantia Nigra	brain
22	chr6:150087800-150094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:150087800-150101600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:150087800-150112000	Weak transcription	Right Ventricle	heart
25	chr6:150087800-150112400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr6:150088000-150096600	Weak transcription	A549	lung
27	chr6:150088000-150096600	Weak transcription	NHEK	skin
28	chr6:150088000-150099600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr6:150088000-150102400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:150088000-150111200	Weak transcription	Brain Hippocampus Middle	brain
31	chr6:150088000-150112000	Weak transcription	Colon Smooth Muscle	Colon
32	chr6:150088000-150123400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr6:150088000-150160400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr6:150088200-150106000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr6:150088200-150115600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:150088800-150094600	Weak transcription	Fetal Brain Female	brain
37	chr6:150088800-150096600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:150088800-150112000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:150089000-150100200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr6:150090200-150105800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:150090400-150100600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:150090800-150094400	Strong transcription	GM12878-XiMat	blood
43	chr6:150090800-150104600	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr6:150090800-150106000	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr6:150090800-150106000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr6:150091000-150094400	Strong transcription	NHDF-Ad	bronchial
47	chr6:150091000-150095400	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr6:150091000-150097800	Strong transcription	Thymus	Thymus
49	chr6:150091000-150098400	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr6:150091000-150098600	Strong transcription	HSMM	muscle

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