Variant report

Variant	nsv1035278
Chromosome Location	chr10:89629273-89641293
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:89638569-89639130	K562	blood:	n/a	n/a
2	ATF1	chr10:89638697-89639079	K562	blood:	n/a	n/a
3	BCLAF1	chr10:89638664-89639157	K562	blood:	n/a	n/a
4	BHLHE40	chr10:89632799-89632804	K562	blood:	n/a	n/a
5	CBX3	chr10:89638705-89639172	K562	blood:	n/a	n/a
6	CBX3	chr10:89638725-89639060	K562	blood:	n/a	n/a
7	CCNT2	chr10:89638737-89639000	K562	blood:	n/a	chr10:89638935-89638955
8	CEBPB	chr10:89635985-89636266	A549	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
9	CEBPB	chr10:89638870-89639070	K562	blood:	n/a	n/a
10	CEBPB	chr10:89635900-89636337	A549	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
11	CEBPB	chr10:89635970-89636287	IMR90	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
12	CEBPB	chr10:89637658-89637806	HepG2	liver:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
13	CEBPB	chr10:89638808-89639206	K562	blood:	n/a	n/a
14	CEBPB	chr10:89637619-89637930	K562	blood:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
15	CEBPB	chr10:89635944-89636282	K562	blood:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
16	CEBPB	chr10:89637645-89637830	H1-hESC	embryonic stem cell:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
17	CEBPB	chr10:89637644-89637833	Hela-S3	cervix:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
18	CEBPB	chr10:89635936-89636307	Hela-S3	cervix:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
19	CEBPB	chr10:89638751-89639193	K562	blood:	n/a	n/a
20	CEBPB	chr10:89635960-89636273	HepG2	liver:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
21	CEBPB	chr10:89637633-89637831	IMR90	lung:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
22	CEBPD	chr10:89638647-89639113	K562	blood:	n/a	n/a
23	CHD1	chr10:89629846-89630046	GM12878	blood:	n/a	n/a
24	CTCF	chr10:89633200-89633350	SAEC	small airway:	n/a	n/a
25	CUX1	chr10:89638165-89638309	K562	blood:	n/a	n/a
26	EBF1	chr10:89630614-89630616	GM12878	blood:	n/a	n/a
27	EP300	chr10:89638631-89639190	K562	blood:	n/a	n/a
28	EP300	chr10:89633096-89633126	GM12878	blood:	n/a	n/a
29	EP300	chr10:89638792-89639146	K562	blood:	n/a	n/a
30	FOS	chr10:89629583-89629895	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr10:89630724-89630917	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr10:89636088-89636262	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr10:89635979-89636288	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr10:89636048-89636288	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr10:89629649-89629859	MCF10A-Er-Src	breast:	n/a	n/a
36	GATA1	chr10:89638581-89639416	PBDE	blood:	n/a	chr10:89638938-89638955
37	GATA2	chr10:89638696-89639218	K562	blood:	n/a	chr10:89638938-89638955
38	GATA3	chr10:89636847-89636903	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr10:89630541-89630811	SH-SY5Y	brain:	n/a	chr10:89630679-89630696 chr10:89630678-89630687 chr10:89630678-89630687
40	HEY1	chr10:89639047-89639283	K562	blood:	n/a	n/a
41	IRF1	chr10:89635822-89635879	K562	blood:	n/a	n/a
42	IRF1	chr10:89638489-89639075	K562	blood:	n/a	n/a
43	IRF1	chr10:89630577-89630641	K562	blood:	n/a	n/a
44	IRF1	chr10:89638350-89639080	K562	blood:	n/a	n/a
45	JUN	chr10:89638648-89638982	K562	blood:	n/a	n/a
46	JUND	chr10:89637719-89637793	HepG2	liver:	n/a	n/a
47	JUND	chr10:89638713-89639104	K562	blood:	n/a	n/a
48	KAP1	chr10:89638686-89639105	U2OS	brain:	n/a	n/a
49	MAFF	chr10:89629968-89630259	HepG2	liver:	n/a	chr10:89630098-89630116
50	MAFF	chr10:89638433-89638979	K562	blood:	n/a	chr10:89638614-89638632

No.	Distal block	Cell Line	Cell type
1	chr10:89628472..89630169-chr10:89642973..89645444,2	K562	blood:
2	chr10:89628331..89631690-chr10:89632886..89636887,5	MCF-7	breast:
3	chr10:89632106..89634679-chr10:89635218..89637761,3	MCF-7	breast:
4	chr10:89627960..89634049-chr10:89634179..89640530,8	K562	blood:
5	chr10:89640838..89642681-chr10:89647239..89649894,3	K562	blood:
6	chr10:89630597..89633078-chr10:89635123..89637172,2	MCF-7	breast:
7	chr10:89627048..89629019-chr10:89631649..89634484,2	K562	blood:
8	chr10:89628331..89631690-chr10:89632886..89636887,5	MCF-7	breast:
9	chr10:89630068..89631816-chr10:89794611..89796207,2	MCF-7	breast:
10	chr10:89622936..89626124-chr10:89632043..89636497,5	MCF-7	breast:
11	chr10:89639384..89642070-chr10:89695863..89697662,2	K562	blood:
12	chr10:89632106..89634679-chr10:89635218..89637761,3	MCF-7	breast:
13	chr10:89619679..89625045-chr10:89627844..89633340,9	K562	blood:
14	chr10:89639033..89641731-chr10:89644524..89647018,2	K562	blood:
15	chr10:89623575..89625821-chr10:89638981..89641950,2	K562	blood:
16	chr10:89629893..89635065-chr10:89636010..89640351,6	K562	blood:
17	chr10:89620447..89623271-chr10:89637766..89641518,4	MCF-7	breast:
18	chr10:89630597..89633078-chr10:89635123..89637172,2	MCF-7	breast:
19	chr10:89621343..89626061-chr10:89634894..89638873,7	K562	blood:
20	chr10:89619679..89625889-chr10:89627245..89632129,8	K562	blood:
21	chr10:89576887..89579810-chr10:89632591..89635220,2	K562	blood:
22	chr10:89631936..89633868-chr10:90147243..90149574,2	MCF-7	breast:
23	chr10:89638682..89641996-chr10:89653428..89657390,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPSS2-2	chr10:89638449-89638780	ENSG00000224745.1
2	lnc-PAPSS2-2	chr10:89640057-89640184	ENSG00000224745.1
3	lnc-PAPSS2-2	chr10:89639829-89639867	ENSG00000224745.1

Variant related genes	Relation type
ENSG00000224745	TF binding region
ENSG00000227268	chromatin interactions
ENSG00000138138	chromatin interactions
ENSG00000224745	chromatin interactions
ENSG00000171862	chromatin interactions
ENSG00000223820	chromatin interactions

Extended variants
information (count: 427 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561183127	chr10:89629275-89629276	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs143282226	chr10:89629366-89629367	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs536808682	chr10:89629443-89629444	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576713505	chr10:89629445-89629446	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs543411274	chr10:89629449-89629450	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs116127902	chr10:89629454-89629455	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529888128	chr10:89629468-89629469	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs577382283	chr10:89629529-89629530	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs183038945	chr10:89629532-89629533	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs187738147	chr10:89629580-89629581	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs192402789	chr10:89629602-89629603	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs36090221	chr10:89629651-89629652	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs182950865	chr10:89629825-89629826	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs563399210	chr10:89629919-89629920	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530839654	chr10:89629921-89629922	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs551727305	chr10:89629988-89629989	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs187691147	chr10:89630018-89630019	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532227325	chr10:89630019-89630020	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs552036141	chr10:89630020-89630021	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377425393	chr10:89630036-89630037	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs534350769	chr10:89630043-89630044	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs11202593	chr10:89630053-89630054	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs546269438	chr10:89630083-89630084	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568192325	chr10:89630089-89630090	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs74754799	chr10:89630142-89630143	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555154357	chr10:89630150-89630151	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576613196	chr10:89630179-89630180	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs537760461	chr10:89630233-89630234	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs558956054	chr10:89630398-89630399	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35161364	chr10:89630424-89630425	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs192655554	chr10:89630437-89630438	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs559879058	chr10:89630481-89630482	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs367799770	chr10:89630483-89630484	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs574887412	chr10:89630520-89630521	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs184313731	chr10:89630526-89630527	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs139554020	chr10:89630536-89630537	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs60706946	chr10:89630537-89630538	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs115656016	chr10:89630550-89630551	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs376409281	chr10:89630566-89630567	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574492533	chr10:89630582-89630583	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7085328	chr10:89630650-89630651	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564069698	chr10:89630721-89630722	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs528071471	chr10:89630728-89630729	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370114925	chr10:89630729-89630730	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs546228864	chr10:89630840-89630841	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs192836744	chr10:89630881-89630882	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs148593767	chr10:89630916-89630917	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs200750915	chr10:89630921-89630922	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs142921964	chr10:89630933-89630934	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs553935180	chr10:89630963-89630964	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Glioblastoma multiforme	19115005	CNVD
Prostate cancer	21147910	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	20020426	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22065749	CNVD
Cancer	22000013	CNVD
Colon cancer	22065749	CNVD
Endometrial cancer	22065749	CNVD
Lung cancer	20668451	CNVD
Breast cancer	17634833	CNVD
Cancer	20215515	CNVD
Glioblastoma multiforme	21727940	CNVD
Prostate cancer	19363497	CNVD
Prostate cancer	17700571	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20964600	CNVD
Endometrial cancer	19261849	CNVD
Central neurocytomas	17123091	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD

Chromatin state (count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89621200-89630800	Active TSS	Aorta	Aorta
2	chr10:89621400-89629800	Active TSS	Ovary	ovary
3	chr10:89621600-89629800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:89621800-89630000	Active TSS	Stomach Smooth Muscle	stomach
5	chr10:89621800-89630600	Active TSS	NHLF	lung
6	chr10:89621800-89632400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:89621800-89632400	Active TSS	GM12878-XiMat	blood
8	chr10:89623200-89629400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr10:89624200-89631800	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr10:89624400-89646400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:89624800-89631200	Weak transcription	Spleen	Spleen
12	chr10:89625600-89663000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:89625800-89632400	Weak transcription	Small Intestine	intestine
14	chr10:89627200-89629800	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr10:89627200-89630600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:89627200-89645800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr10:89627400-89630000	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr10:89627400-89630800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr10:89627400-89631600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr10:89627400-89638200	Weak transcription	Placenta	Placenta
21	chr10:89627600-89629400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:89627600-89645600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:89628000-89629400	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr10:89628000-89629400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr10:89628000-89635200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr10:89628200-89629400	Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr10:89628200-89629400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr10:89628200-89635800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr10:89628200-89646200	Weak transcription	Fetal Muscle Leg	muscle
30	chr10:89628200-89646600	Weak transcription	Colonic Mucosa	Colon
31	chr10:89628400-89629800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr10:89628400-89633800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr10:89628400-89637800	Weak transcription	Fetal Intestine Small	intestine
34	chr10:89628400-89662000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr10:89628600-89629400	Enhancers	Fetal Brain Male	brain
36	chr10:89628600-89629400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr10:89628600-89629600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:89628600-89629600	Enhancers	Duodenum Mucosa	Duodenum
39	chr10:89628600-89629800	Enhancers	Primary B cells from peripheral blood	blood
40	chr10:89628600-89629800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:89628600-89629800	Enhancers	Brain Germinal Matrix	brain
42	chr10:89628600-89629800	Weak transcription	Fetal Heart	heart
43	chr10:89628600-89629800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr10:89628600-89629800	Active TSS	NHDF-Ad	bronchial
45	chr10:89628600-89630000	Enhancers	NH-A	brain
46	chr10:89628600-89630600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr10:89628600-89630800	Weak transcription	Brain Substantia Nigra	brain
48	chr10:89628600-89631200	Enhancers	Colon Smooth Muscle	Colon
49	chr10:89628600-89631200	Enhancers	HepG2	liver
50	chr10:89628600-89631400	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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