Variant report

Variant	nsv610171
Chromosome Location	chr8:8290294-8328101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:122)
Chromatin interactive
region (count:37)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8314706-8315018	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8324363-8325247	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8318936-8319027	HepG2	liver:	n/a	n/a
4	ATF2	chr8:8324529-8324992	GM12878	blood:	n/a	n/a
5	ATF2	chr8:8293199-8293483	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:8310031-8310713	GM12878	blood:	n/a	n/a
7	ATF2	chr8:8310015-8310665	GM12878	blood:	n/a	n/a
8	ATF2	chr8:8324550-8324879	GM12878	blood:	n/a	n/a
9	BACH1	chr8:8313375-8313563	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:8310182-8310550	GM12878	blood:	n/a	n/a
11	BATF	chr8:8310225-8310548	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:8310128-8310497	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:8310249-8310487	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:8310038-8310609	GM12878	blood:	n/a	n/a
15	BCLAF1	chr8:8310124-8310538	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:8324440-8325002	HepG2	liver:	n/a	n/a
17	BHLHE40	chr8:8313440-8313517	K562	blood:	n/a	n/a
18	BHLHE40	chr8:8313428-8313566	A549	lung:	n/a	n/a
19	BHLHE40	chr8:8310177-8310477	GM12878	blood:	n/a	n/a
20	BRCA1	chr8:8313642-8313649	HepG2	liver:	n/a	n/a
21	CBX3	chr8:8293104-8293495	K562	blood:	n/a	n/a
22	CBX3	chr8:8298667-8299528	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:8293131-8293493	K562	blood:	n/a	n/a
24	CBX3	chr8:8293081-8293537	HCT-116	colon:	n/a	n/a
25	CBX3	chr8:8298711-8299537	HCT-116	colon:	n/a	n/a
26	CBX3	chr8:8293023-8293525	HCT-116	colon:	n/a	n/a
27	CEBPB	chr8:8313392-8313576	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:8309492-8309730	IMR90	lung:	n/a	chr8:8309599-8309610
29	CEBPB	chr8:8313314-8314082	A549	lung:	n/a	chr8:8313825-8313836
30	CEBPB	chr8:8305274-8305363	A549	lung:	n/a	n/a
31	CEBPB	chr8:8313367-8313677	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:8309467-8309731	A549	lung:	n/a	chr8:8309599-8309610
33	CEBPB	chr8:8309555-8309742	HepG2	liver:	n/a	chr8:8309599-8309610
34	CEBPB	chr8:8324596-8325001	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:8313772-8313879	H1-hESC	embryonic stem cell:	n/a	chr8:8313825-8313836
36	CEBPB	chr8:8307022-8307239	MCF-7	breast:	n/a	n/a
37	CEBPB	chr8:8313296-8314008	Hela-S3	cervix:	n/a	chr8:8313825-8313836
38	CEBPB	chr8:8306900-8307304	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:8313810-8313880	HepG2	liver:	n/a	chr8:8313825-8313836
40	CEBPB	chr8:8313408-8313951	A549	lung:	n/a	chr8:8313825-8313836
41	CHD2	chr8:8313285-8313945	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr8:8324676-8324913	HepG2	liver:	n/a	n/a
43	CHD2	chr8:8309880-8310497	GM12878	blood:	n/a	n/a
44	CTCF	chr8:8313500-8313650	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr8:8300360-8300510	NHEK	skin:	n/a	n/a
46	CTCF	chr8:8316400-8316550	HPF	lung:	n/a	n/a
47	CTCF	chr8:8300344-8300475	NHEK	skin:	n/a	n/a
48	CTCF	chr8:8303180-8303330	GM12869	blood:	n/a	n/a
49	CTCF	chr8:8300320-8300470	HMEC	breast:	n/a	n/a
50	CTCF	chr8:8316480-8316630	HCT-116	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8318774-8318824	HCT-116	colon:	n/a
2	chr8:8318774-8318824	HepG2	liver:	n/a
3	chr8:8318774-8318824	AG09319	gingival:	n/a
4	chr8:8313504-8313554	AG09309	skin:	n/a
5	chr8:8313504-8313554	HMEC	breast:	n/a
6	chr8:8313504-8313554	RPTEC	kidney:	n/a
7	chr8:8318774-8318824	HL-60	blood:	n/a
8	chr8:8318774-8318824	MCF10A-Er-Src	breast:	n/a
9	chr8:8313504-8313554	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:8318774-8318824	BJ	skin:	n/a
11	chr8:8313504-8313554	HCPEpiC	choroid plexus:	n/a
12	chr8:8318774-8318824	HEEpiC	esophagus:	n/a
13	chr8:8313504-8313554	SK-N-SH	brain:	n/a
14	chr8:8318774-8318824	HRE	kidney:	n/a
15	chr8:8318774-8318824	GM12891	blood:	n/a
16	chr8:8313504-8313554	H1-hESC	embryonic stem cell:	embryo
17	chr8:8313504-8313554	NB4	blood:	n/a
18	chr8:8318774-8318824	PFSK-1	brain:	n/a
19	chr8:8318774-8318824	MCF-7	breast:	n/a
20	chr8:8318774-8318824	AG04449	skin:	fetal
21	chr8:8313504-8313554	PANC-1	pancreas:	n/a
22	chr8:8313504-8313554	HCT-116	colon:	n/a
23	chr8:8318774-8318824	GM12892	blood:	n/a
24	chr8:8313504-8313554	HRPEpiC	eye:	n/a
25	chr8:8318774-8318824	HRPEpiC	eye:	n/a
26	chr8:8313504-8313554	HL-60	blood:	n/a
27	chr8:8318774-8318824	SK-N-SH	brain:	n/a
28	chr8:8318774-8318824	SK-N-SH_RA	brain:	n/a
29	chr8:8313504-8313554	HNPCEpiC	eye:	n/a
30	chr8:8313504-8313554	Jurkat	blood:	n/a
31	chr8:8318774-8318824	GM06990	blood:	n/a
32	chr8:8318774-8318824	HAEpiC	amniotic membrane:	n/a
33	chr8:8318774-8318824	Hepatocyte	liver:	n/a
34	chr8:8318774-8318824	K562	blood:	n/a
35	chr8:8313504-8313554	GM12892	blood:	n/a
36	chr8:8318774-8318824	HNPCEpiC	eye:	n/a
37	chr8:8313504-8313554	K562	blood:	n/a
38	chr8:8313504-8313554	U87	brain:	n/a
39	chr8:8313504-8313554	HIPEpiC	eye:	n/a
40	chr8:8313504-8313554	GM12891	blood:	n/a
41	chr8:8318774-8318824	Hela-S3	cervix:	n/a
42	chr8:8318774-8318824	SK-N-MC	brain:	n/a
43	chr8:8318774-8318824	HCPEpiC	choroid plexus:	n/a
44	chr8:8318774-8318824	CMK	blood:	n/a
45	chr8:8318774-8318824	HIPEpiC	eye:	n/a
46	chr8:8313504-8313554	NHDF-neo	bronchial:	n/a
47	chr8:8318774-8318824	NT2-D1	testis:	n/a
48	chr8:8313504-8313554	HepG2	liver:	n/a
49	chr8:8318774-8318824	LNCaP	prostate:	n/a
50	chr8:8313504-8313554	A549	lung:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8242907..8245706-chr8:8295976..8300172,6	MCF-7	breast:
2	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
3	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
4	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
5	chr8:8241927..8245169-chr8:8316549..8319625,5	MCF-7	breast:
6	chr8:8307087..8309406-chr8:8317216..8320167,2	MCF-7	breast:
7	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
8	chr8:8241273..8244866-chr8:8311320..8315481,8	MCF-7	breast:
9	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
10	chr8:8242477..8244553-chr8:8320092..8324260,3	MCF-7	breast:
11	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
12	chr8:8301355..8304096-chr8:8318371..8320187,2	MCF-7	breast:
13	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
14	chr8:8312145..8315725-chr8:8317532..8320911,6	MCF-7	breast:
15	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
16	chr8:8306469..8311532-chr8:8316315..8320180,6	MCF-7	breast:
17	chr8:8243810..8245986-chr8:8307375..8310131,2	MCF-7	breast:
18	chr8:8242445..8245313-chr8:8297878..8301672,4	MCF-7	breast:
19	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
20	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:
21	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
22	chr8:8299017..8300539-chr8:8317523..8321166,3	MCF-7	breast:
23	chr8:8151768..8153956-chr8:8305542..8308270,3	MCF-7	breast:
24	chr8:8242160..8245521-chr8:8318713..8321604,3	MCF-7	breast:
25	chr8:8311665..8315626-chr8:8317447..8320934,9	MCF-7	breast:
26	chr8:8241777..8245267-chr8:8311182..8314962,7	MCF-7	breast:
27	chr8:8317141..8321564-chr8:8323708..8327409,4	MCF-7	breast:
28	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
29	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
30	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
31	chr8:8317671..8320936-chr8:8323021..8325939,5	MCF-7	breast:
32	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
33	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
34	chr8:8237866..8240823-chr8:8310722..8313327,2	MCF-7	breast:
35	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
36	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:
37	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-2	chr8:8314419-8314592	ENSG00000254153
2	lnc-PRAGMIN.1-2	chr8:8318630-8318847	ENSG00000254153
3	lnc-PRAGMIN.1-8	chr8:8327533-8327591	NONHSAT124876
4	lnc-AC068020.1-4	chr8:8322957-8323060	NONHSAT124875
5	lnc-PRAGMIN.1-2	chr8:8315919-8316036	ENSG00000254153

No data

Variant related genes	Relation type
ENSG00000254153	TF binding region
ENSG00000254153	CpG island
ENSG00000182319	chromatin interactions
ENSG00000254153	chromatin interactions

Extended variants
information (count: 2336 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2336 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55712983	chr8:8290296-8290297	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189272477	chr8:8290302-8290303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562464411	chr8:8290305-8290306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180940004	chr8:8290314-8290315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375131013	chr8:8290316-8290317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369650085	chr8:8290340-8290341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138439143	chr8:8290348-8290349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567805461	chr8:8290356-8290357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185946595	chr8:8290425-8290426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373423604	chr8:8290430-8290431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537962271	chr8:8290488-8290489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547178210	chr8:8290490-8290491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2979163	chr8:8290514-8290515	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546319940	chr8:8290585-8290586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147248814	chr8:8290588-8290589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112381464	chr8:8290606-8290607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566461357	chr8:8290611-8290612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113183378	chr8:8290630-8290631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2921091	chr8:8290633-8290634	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556046926	chr8:8290653-8290654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10089015	chr8:8290673-8290674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs76618196	chr8:8290678-8290679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113714897	chr8:8290685-8290686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191319608	chr8:8290688-8290689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577942585	chr8:8290689-8290690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183181164	chr8:8290691-8290692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569540497	chr8:8290693-8290694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562427447	chr8:8290721-8290722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538465361	chr8:8290736-8290737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531540906	chr8:8290759-8290760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541621151	chr8:8290776-8290777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186961013	chr8:8290861-8290862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7818421	chr8:8290881-8290882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547432759	chr8:8290891-8290892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570473479	chr8:8290911-8290912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532917666	chr8:8290924-8290925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549845240	chr8:8290949-8290950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570364223	chr8:8291008-8291009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564110312	chr8:8291050-8291051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536111020	chr8:8291067-8291068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190465911	chr8:8291072-8291073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566231713	chr8:8291098-8291099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182746120	chr8:8291115-8291116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558210671	chr8:8291143-8291144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369177371	chr8:8291144-8291145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11783012	chr8:8291165-8291166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10089651	chr8:8291212-8291213	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs141371543	chr8:8291224-8291225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73184391	chr8:8291241-8291242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112187391	chr8:8291255-8291256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8286200-8292600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:8288800-8290800	Enhancers	HSMMtube	muscle
3	chr8:8289400-8290400	Enhancers	Placenta	Placenta
4	chr8:8289400-8290600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:8289400-8290800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:8289600-8290600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:8291600-8292200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr8:8292600-8293600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:8293600-8294000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:8294000-8298600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:8295800-8297400	Enhancers	Primary B cells from peripheral blood	blood
12	chr8:8295800-8297600	Enhancers	Primary B cells from cord blood	blood
13	chr8:8296000-8296800	Enhancers	Stomach Mucosa	stomach
14	chr8:8296000-8296800	Enhancers	GM12878-XiMat	blood
15	chr8:8296000-8297000	Enhancers	Fetal Intestine Small	intestine
16	chr8:8296200-8296400	Enhancers	Fetal Lung	lung
17	chr8:8296200-8296800	Enhancers	Fetal Intestine Large	intestine
18	chr8:8296200-8303000	Enhancers	Placenta Amnion	Placenta Amnion
19	chr8:8296400-8296600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:8296400-8296600	Enhancers	Duodenum Mucosa	Duodenum
21	chr8:8296400-8296800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:8296400-8296800	Enhancers	Esophagus	oesophagus
23	chr8:8296400-8300000	Weak transcription	Fetal Lung	lung
24	chr8:8296600-8296800	Enhancers	Gastric	stomach
25	chr8:8296600-8297800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr8:8296600-8298200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:8296800-8298200	Weak transcription	Stomach Mucosa	stomach
28	chr8:8296800-8298600	Weak transcription	Esophagus	oesophagus
29	chr8:8296800-8298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:8296800-8298800	Weak transcription	Gastric	stomach
31	chr8:8296800-8300400	Weak transcription	Fetal Intestine Large	intestine
32	chr8:8297000-8297400	Weak transcription	Fetal Intestine Small	intestine
33	chr8:8297400-8299600	Enhancers	Fetal Intestine Small	intestine
34	chr8:8297800-8300600	Enhancers	Duodenum Mucosa	Duodenum
35	chr8:8298200-8298800	Enhancers	Stomach Mucosa	stomach
36	chr8:8298200-8298800	Enhancers	NHEK	skin
37	chr8:8298200-8300800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:8298200-8302400	Enhancers	Placenta	Placenta
39	chr8:8298600-8300600	Enhancers	HMEC	breast
40	chr8:8298600-8300800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:8298600-8300800	Enhancers	Esophagus	oesophagus
42	chr8:8298600-8301000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:8298800-8299000	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr8:8298800-8299000	Flanking Active TSS	Stomach Mucosa	stomach
45	chr8:8298800-8299200	Enhancers	Lung	lung
46	chr8:8298800-8299200	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr8:8298800-8299400	Enhancers	Fetal Thymus	thymus
48	chr8:8298800-8299400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:8298800-8299600	Enhancers	HSMMtube	muscle
50	chr8:8298800-8299800	Flanking Active TSS	NHEK	skin

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