Variant report

Variant	nsv610189
Chromosome Location	chr8:8590437-8664940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1576)
CpG islands
(count:671)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1576 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8662803-8662910	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8663637-8664197	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8646553-8646667	K562	blood:	n/a	n/a
4	ARID3A	chr8:8664446-8665279	K562	blood:	n/a	n/a
5	ARID3A	chr8:8635226-8635514	K562	blood:	n/a	n/a
6	ATF1	chr8:8657292-8657474	K562	blood:	n/a	n/a
7	ATF1	chr8:8664546-8664876	K562	blood:	n/a	n/a
8	ATF1	chr8:8648618-8648890	K562	blood:	n/a	n/a
9	ATF2	chr8:8602083-8602540	GM12878	blood:	n/a	n/a
10	ATF2	chr8:8610416-8611030	GM12878	blood:	n/a	n/a
11	ATF2	chr8:8654504-8655116	GM12878	blood:	n/a	n/a
12	ATF2	chr8:8610412-8611045	GM12878	blood:	n/a	n/a
13	ATF3	chr8:8639637-8640217	A549	lung:	n/a	n/a
14	ATF3	chr8:8654560-8654914	K562	blood:	n/a	chr8:8654727-8654740
15	ATF3	chr8:8663489-8664131	A549	lung:	n/a	n/a
16	ATF3	chr8:8663544-8664086	A549	lung:	n/a	n/a
17	BATF	chr8:8602155-8602419	GM12878	blood:	n/a	n/a
18	BATF	chr8:8594412-8594844	GM12878	blood:	n/a	chr8:8594646-8594657 chr8:8594647-8594657
19	BATF	chr8:8610529-8610866	GM12878	blood:	n/a	n/a
20	BATF	chr8:8610497-8610925	GM12878	blood:	n/a	n/a
21	BATF	chr8:8594497-8594769	GM12878	blood:	n/a	chr8:8594646-8594657 chr8:8594647-8594657
22	BCL11A	chr8:8602157-8602357	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:8610556-8610896	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:8610430-8610992	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:8602151-8602466	GM12878	blood:	n/a	n/a
26	BCL3	chr8:8663492-8664118	A549	lung:	n/a	n/a
27	BCL3	chr8:8663474-8664218	A549	lung:	n/a	n/a
28	BCL3	chr8:8639320-8640346	A549	lung:	n/a	n/a
29	BCL3	chr8:8639354-8639932	A549	lung:	n/a	n/a
30	BCLAF1	chr8:8608232-8608593	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:8610434-8610900	GM12878	blood:	n/a	n/a
32	BCLAF1	chr8:8601984-8602545	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:8610456-8611005	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:8654776-8655254	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:8663629-8663903	HepG2	liver:	n/a	chr8:8663696-8663712
36	BHLHE40	chr8:8663597-8664062	HepG2	liver:	n/a	chr8:8663696-8663712
37	BHLHE40	chr8:8662947-8663309	HepG2	liver:	n/a	n/a
38	BHLHE40	chr8:8594381-8594738	K562	blood:	n/a	n/a
39	BHLHE40	chr8:8664514-8664896	K562	blood:	n/a	n/a
40	BHLHE40	chr8:8594387-8594712	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:8610461-8610970	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:8611852-8612213	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:8611870-8612221	K562	blood:	n/a	n/a
44	BHLHE40	chr8:8654901-8655245	K562	blood:	n/a	n/a
45	BHLHE40	chr8:8608239-8608505	K562	blood:	n/a	n/a
46	BHLHE40	chr8:8635240-8635558	K562	blood:	n/a	n/a
47	BHLHE40	chr8:8594092-8594278	A549	lung:	n/a	n/a
48	BRCA1	chr8:8647804-8647912	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr8:8654760-8654869	GM12878	blood:	n/a	n/a
50	BRCA1	chr8:8641431-8641507	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8652454-8652504	HRPEpiC	eye:	n/a
2	chr8:8643280-8643330	NHBE	bronchial:	n/a
3	chr8:8640017-8640067	HUVEC	blood vessel:	n/a
4	chr8:8643280-8643330	HCF	heart:	n/a
5	chr8:8643280-8643330	HCT-116	colon:	n/a
6	chr8:8639926-8639976	AoSMC	blood vessel:	n/a
7	chr8:8643280-8643330	HIPEpiC	eye:	n/a
8	chr8:8652379-8652429	T-47D	breast:	n/a
9	chr8:8639926-8639976	HRE	kidney:	n/a
10	chr8:8643280-8643330	AG09319	gingival:	n/a
11	chr8:8647440-8647490	HRPEpiC	eye:	n/a
12	chr8:8601022-8601072	HIPEpiC	eye:	n/a
13	chr8:8621874-8621924	MCF10A-Er-Src	breast:	n/a
14	chr8:8643280-8643330	SKMC	muscle:	n/a
15	chr8:8639926-8639976	SK-N-SH	brain:	n/a
16	chr8:8630364-8630414	HepG2	liver:	n/a
17	chr8:8639926-8639976	AG04449	skin:	fetal
18	chr8:8630364-8630414	AG04450	lung:	fetal
19	chr8:8621874-8621924	GM12891	blood:	n/a
20	chr8:8652379-8652429	RPTEC	kidney:	n/a
21	chr8:8640017-8640067	IMR90	lung:	fetal
22	chr8:8639450-8639500	GM12878	blood:	n/a
23	chr8:8621874-8621924	HL-60	blood:	n/a
24	chr8:8652347-8652397	HRE	kidney:	n/a
25	chr8:8601022-8601072	A549	lung:	n/a
26	chr8:8639450-8639500	Jurkat	blood:	n/a
27	chr8:8630364-8630414	HCM	heart:	n/a
28	chr8:8652347-8652397	HCM	heart:	n/a
29	chr8:8630364-8630414	HCT-116	colon:	n/a
30	chr8:8647440-8647490	LNCaP	prostate:	n/a
31	chr8:8652379-8652429	CMK	blood:	n/a
32	chr8:8630364-8630414	AoSMC	blood vessel:	n/a
33	chr8:8621874-8621924	SK-N-SH_RA	brain:	n/a
34	chr8:8639450-8639500	GM19239	blood:	n/a
35	chr8:8621874-8621924	NH-A	brain:	n/a
36	chr8:8621874-8621924	Hepatocyte	liver:	n/a
37	chr8:8621874-8621924	AG09309	skin:	n/a
38	chr8:8621874-8621924	HEK293	kidney:	embryo
39	chr8:8652347-8652397	K562	blood:	n/a
40	chr8:8621874-8621924	Caco-2	colon:	n/a
41	chr8:8639450-8639500	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:8630364-8630414	K562	blood:	n/a
43	chr8:8639926-8639976	HAEpiC	amniotic membrane:	n/a
44	chr8:8640017-8640067	GM12892	blood:	n/a
45	chr8:8601022-8601072	NB4	blood:	n/a
46	chr8:8652379-8652429	HEK293	kidney:	embryo
47	chr8:8652379-8652429	HUVEC	blood vessel:	n/a
48	chr8:8652454-8652504	GM06990	blood:	n/a
49	chr8:8601022-8601072	AG09309	skin:	n/a
50	chr8:8643280-8643330	PFSK-1	brain:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8527332..8529283-chr8:8594084..8595110,9	K562	blood:
2	chr8:8617914..8619415-chr8:8620497..8623459,2	K562	blood:
3	chr8:8637196..8637781-chr8:8800088..8800758,2	MCF-7	breast:
4	chr8:8608326..8608981-chr8:9195964..9196742,2	MCF-7	breast:
5	chr8:8655376..8657753-chr8:8661368..8663526,2	MCF-7	breast:
6	chr8:8608085..8608900-chr8:8846417..8847265,2	MCF-7	breast:
7	chr8:8607817..8608748-chr8:9007897..9008818,2	MCF-7	breast:
8	chr8:8655376..8657753-chr8:8661368..8663526,2	MCF-7	breast:
9	chr8:8527839..8528754-chr8:8592246..8592999,2	K562	blood:
10	chr8:8242378..8243902-chr8:8594357..8596139,2	MCF-7	breast:
11	chr8:8647143..8649997-chr8:8748170..8750908,2	MCF-7	breast:
12	chr8:8607923..8608592-chr8:9007837..9008750,3	K562	blood:
13	chr8:8645586..8647126-chr8:8650976..8652774,2	K562	blood:
14	chr8:8641971..8645218-chr8:8645421..8648443,3	MCF-7	breast:
15	chr8:8635419..8638505-chr8:8640387..8644598,4	K562	blood:
16	chr8:8648185..8650191-chr8:8651639..8653893,2	MCF-7	breast:
17	chr8:8640474..8642635-chr8:8745832..8748288,2	MCF-7	breast:
18	chr8:8538997..8539534-chr8:8594174..8595039,2	MCF-7	breast:
19	chr8:8527493..8529178-chr8:8594079..8595134,11	MCF-7	breast:
20	chr8:8637005..8638649-chr8:8642438..8644598,2	K562	blood:
21	chr8:8607912..8608860-chr8:8887402..8888108,2	K562	blood:
22	chr8:8663729..8665555-chr8:8666802..8669235,2	K562	blood:
23	chr8:8608069..8609942-chr8:8861282..8862933,2	MCF-7	breast:
24	chr8:8636902..8637804-chr8:8750649..8751239,2	MCF-7	breast:
25	chr8:8622225..8624957-chr8:8625009..8627132,2	MCF-7	breast:
26	chr8:8636919..8637702-chr8:8799876..8800811,2	MCF-7	breast:
27	chr8:8637005..8638649-chr8:8642438..8644598,2	K562	blood:
28	chr8:8579801..8581466-chr8:8590103..8593043,2	MCF-7	breast:
29	chr8:8637281..8637804-chr8:8820490..8821301,2	MCF-7	breast:
30	chr8:8617914..8619415-chr8:8620497..8623459,2	K562	blood:
31	chr8:8638841..8640661-chr8:8641963..8645166,3	K562	blood:
32	chr8:8527797..8529806-chr8:8592444..8595839,3	MCF-7	breast:
33	chr8:8645586..8647126-chr8:8650976..8652774,2	K562	blood:
34	chr8:8599224..8601341-chr8:8748933..8751645,2	MCF-7	breast:
35	chr8:8630359..8632288-chr8:8847032..8849956,2	MCF-7	breast:
36	chr8:8634836..8637648-chr8:8864652..8866241,2	K562	blood:
37	chr8:8648185..8650191-chr8:8651639..8653893,2	MCF-7	breast:
38	chr8:8641971..8645218-chr8:8645421..8648443,3	MCF-7	breast:
39	chr8:8607965..8608861-chr8:8846540..8847483,5	K562	blood:
40	chr8:8636970..8637812-chr8:8846579..8847342,2	MCF-7	breast:
41	chr8:8635419..8638505-chr8:8640387..8644598,4	K562	blood:
42	chr8:8622225..8624957-chr8:8625009..8627132,2	MCF-7	breast:
43	chr8:8637079..8641758-chr8:8747812..8752273,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFHAS1-1	chr8:8639616-8639989	ENSG00000254367
2	lnc-MFHAS1-1	chr8:8611510-8611618	ENSG00000254367
3	lnc-MFHAS1-1	chr8:8614686-8614826	ENSG00000254367

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MFHAS1	hsa-miR-26b-5p	chr8:8643277-8643270
2	MFHAS1	hsa-miR-32-5p	chr8:8643007-8643000
3	MFHAS1	hsa-miR-125b-5p	chr8:8643228-8643253
4	MFHAS1	hsa-miR-125b-5p	chr8:8643234-8643227
5	MFHAS1	hsa-miR-26a-5p	chr8:8643277-8643270
6	MFHAS1	hsa-miR-17-5p	chr8:8642568-8642592
7	MFHAS1	hsa-miR-26a-5p	chr8:8643271-8643292
8	MFHAS1	hsa-miR-32-5p	chr8:8643001-8643029
9	MFHAS1	hsa-miR-26b-5p	chr8:8643271-8643291

Variant related genes	Relation type
ENSG00000254367	TF binding region
ENSG00000254367	CpG island
ENSG00000254367	chromatin interactions
ENSG00000147324	chromatin interactions
ENSG00000173281	chromatin interactions

Extended variants
information (count: 4285 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:4285 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143467733	chr8:8591010-8591011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs28716524	chr8:8591073-8591074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200242384	chr8:8591075-8591076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371834356	chr8:8591080-8591081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200425814	chr8:8591081-8591082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200599569	chr8:8591082-8591083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1969408	chr8:8591093-8591094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575730017	chr8:8591135-8591136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548998986	chr8:8591136-8591137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561317362	chr8:8591143-8591144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574893766	chr8:8591146-8591147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13264411	chr8:8591149-8591150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540596461	chr8:8591153-8591154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559704873	chr8:8591169-8591170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528352575	chr8:8591219-8591220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs386721997	chr8:8591240-8591241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149951892	chr8:8591242-8591243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58123604	chr8:8591243-8591244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369541926	chr8:8591245-8591246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564922702	chr8:8591257-8591258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117131595	chr8:8591274-8591275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550408256	chr8:8591275-8591276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566983905	chr8:8591286-8591287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141577942	chr8:8591291-8591292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546162469	chr8:8591309-8591310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112025974	chr8:8591319-8591320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552869537	chr8:8591330-8591331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374150829	chr8:8591351-8591352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538951109	chr8:8591360-8591361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559149041	chr8:8591368-8591369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575749723	chr8:8591370-8591371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117424193	chr8:8591377-8591378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555114241	chr8:8591380-8591381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541492203	chr8:8591382-8591383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185571291	chr8:8591442-8591443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370542547	chr8:8591450-8591451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190446122	chr8:8591478-8591479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544972665	chr8:8591482-8591483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565141775	chr8:8591494-8591495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530629264	chr8:8591495-8591496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550327740	chr8:8591496-8591497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560673329	chr8:8591517-8591518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181629109	chr8:8591529-8591530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74433718	chr8:8591546-8591547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76079102	chr8:8591553-8591554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538580015	chr8:8591578-8591579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186749838	chr8:8591628-8591629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77717027	chr8:8591632-8591633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538076664	chr8:8591645-8591646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76480596	chr8:8591657-8591658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

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
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8591000-8594200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:8594000-8594200	Enhancers	Duodenum Mucosa	Duodenum
3	chr8:8594000-8594200	Enhancers	A549	lung
4	chr8:8594000-8594600	Enhancers	NHEK	skin
5	chr8:8594200-8594400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
6	chr8:8594200-8594400	Enhancers	Placenta Amnion	Placenta Amnion
7	chr8:8594200-8594400	Enhancers	Hela-S3	cervix
8	chr8:8594200-8594600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:8594200-8594600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr8:8594200-8594600	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr8:8594200-8594600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:8594200-8594600	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr8:8594200-8594600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr8:8594200-8594600	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr8:8594200-8594600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:8594200-8594600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:8594200-8594600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:8594200-8594600	Enhancers	Liver	Liver
19	chr8:8594200-8594600	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr8:8594200-8594600	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:8594200-8594800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr8:8594200-8594800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
23	chr8:8594200-8594800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
24	chr8:8594200-8594800	Flanking Active TSS	A549	lung
25	chr8:8594200-8595000	Enhancers	Stomach Mucosa	stomach
26	chr8:8594200-8595000	Enhancers	HMEC	breast
27	chr8:8594400-8594600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr8:8594400-8594600	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:8594400-8594600	Flanking Active TSS	Aorta	Aorta
30	chr8:8594400-8594600	Enhancers	Fetal Intestine Small	intestine
31	chr8:8594400-8594800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr8:8594400-8594800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr8:8594400-8594800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
34	chr8:8594400-8594800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:8594400-8594800	Bivalent Enhancer	NH-A	brain
36	chr8:8594400-8595000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:8594600-8594800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr8:8594600-8594800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:8594600-8594800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr8:8594600-8594800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
41	chr8:8594600-8594800	Enhancers	Duodenum Mucosa	Duodenum
42	chr8:8594600-8594800	Bivalent Enhancer	Fetal Intestine Small	intestine
43	chr8:8594600-8594800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
44	chr8:8594600-8595000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:8594600-8595000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:8594600-8595000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:8594600-8595000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:8594600-8595000	Enhancers	Fetal Lung	lung
49	chr8:8594600-8595000	Bivalent Enhancer	HSMM	muscle
50	chr8:8594800-8595000	Enhancers	A549	lung

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