Variant report

Variant	nsv969380
Chromosome Location	chr6:31797103-31797836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31797611-31798303	K562	blood:	n/a	n/a
2	BACH1	chr6:31797607-31799758	K562	blood:	n/a	n/a
3	BHLHE40	chr6:31797739-31798242	GM12878	blood:	n/a	n/a
4	CBX3	chr6:31794192-31798316	K562	blood:	n/a	chr6:31794873-31794884
5	CCNT2	chr6:31797488-31797860	K562	blood:	n/a	n/a
6	CHD1	chr6:31797607-31798081	GM12878	blood:	n/a	n/a
7	CHD2	chr6:31797617-31800276	K562	blood:	n/a	chr6:31798298-31798308
8	CTCF	chr6:31797738-31797991	HepG2	liver:	n/a	n/a
9	CTCF	chr6:31797800-31797950	GM12865	blood:	n/a	n/a
10	CTCF	chr6:31797760-31797910	GM12873	blood:	n/a	n/a
11	CTCF	chr6:31797814-31797950	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr6:31797780-31797930	GM12866	blood:	n/a	n/a
13	CTCF	chr6:31797728-31798005	A549	lung:	n/a	n/a
14	CTCF	chr6:31797824-31797953	LNCaP	prostate:	n/a	n/a
15	CTCF	chr6:31797760-31797910	HEK293	kidney:	n/a	n/a
16	CTCF	chr6:31797700-31797850	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr6:31797680-31797830	HAc	cerebellar:	n/a	n/a
18	CTCF	chr6:31797786-31797998	Medullo	brain:	n/a	n/a
19	CTCF	chr6:31797800-31797950	HMF	breast:	n/a	n/a
20	CTCF	chr6:31797800-31797950	AG04450	lung:	n/a	n/a
21	CTCF	chr6:31797820-31797970	GM12801	blood:	n/a	n/a
22	CTCF	chr6:31797834-31797963	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:31797780-31797930	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr6:31797800-31797950	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr6:31797720-31797870	HPF	lung:	n/a	n/a
26	CTCF	chr6:31797819-31797992	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr6:31797803-31797959	K562	blood:	n/a	n/a
28	CTCF	chr6:31797820-31797970	AG10803	skin:	n/a	n/a
29	CTCF	chr6:31797800-31797950	GM12868	blood:	n/a	n/a
30	CTCF	chr6:31797340-31797490	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr6:31797760-31797910	HepG2	liver:	n/a	n/a
32	CTCF	chr6:31797760-31797910	GM12872	blood:	n/a	n/a
33	CTCF	chr6:31797794-31798015	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr6:31797820-31798110	HPF	lung:	n/a	n/a
35	CTCF	chr6:31797720-31797870	WI-38	lung:	n/a	n/a
36	CTCF	chr6:31797792-31797978	GM12878	blood:	n/a	n/a
37	CTCF	chr6:31797553-31798210	A549	lung:	n/a	n/a
38	CTCF	chr6:31797760-31797910	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr6:31797263-31797355	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:31797800-31797950	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr6:31797820-31797970	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:31797760-31797910	GM06990	blood:	n/a	n/a
43	CTCF	chr6:31797336-31797341	GM10266	blood:	n/a	n/a
44	CTCF	chr6:31797760-31797910	GM12870	blood:	n/a	n/a
45	CTCF	chr6:31797740-31797890	GM12875	blood:	n/a	n/a
46	CTCF	chr6:31797800-31797950	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr6:31797780-31797930	GM12871	blood:	n/a	n/a
48	CTCF	chr6:31797831-31797936	Lung_OC	lung:	n/a	n/a
49	CTCF	chr6:31797820-31797970	BJ	skin:	n/a	n/a
50	CTCF	chr6:31797760-31797910	BJ	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31797416-31797466	SAEC	small airway:	n/a
2	chr6:31797416-31797466	HAEpiC	amniotic membrane:	n/a
3	chr6:31797421-31797471	AG04450	lung:	fetal
4	chr6:31797821-31797871	AG09309	skin:	n/a
5	chr6:31797821-31797871	HMEC	breast:	n/a
6	chr6:31797821-31797871	LNCaP	prostate:	n/a
7	chr6:31797821-31797871	Hepatocyte	liver:	n/a
8	chr6:31797821-31797871	SAEC	small airway:	n/a
9	chr6:31797821-31797871	GM12891	blood:	n/a
10	chr6:31797821-31797871	AG09319	gingival:	n/a
11	chr6:31797416-31797466	Hela-S3	cervix:	n/a
12	chr6:31797416-31797466	BE2_C	brain:	n/a
13	chr6:31797821-31797871	HUVEC	blood vessel:	n/a
14	chr6:31797416-31797466	HCPEpiC	choroid plexus:	n/a
15	chr6:31797416-31797466	HMEC	breast:	n/a
16	chr6:31797421-31797471	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:31797421-31797471	T-47D	breast:	n/a
18	chr6:31797416-31797466	SK-N-SH_RA	brain:	n/a
19	chr6:31797421-31797471	PrEC	prostate:	n/a
20	chr6:31797416-31797466	MCF10A-Er-Src	breast:	n/a
21	chr6:31797421-31797471	SK-N-SH	brain:	n/a
22	chr6:31797416-31797466	HCT-116	colon:	n/a
23	chr6:31797416-31797466	H1-hESC	embryonic stem cell:	embryo
24	chr6:31797821-31797871	Jurkat	blood:	n/a
25	chr6:31797416-31797466	PFSK-1	brain:	n/a
26	chr6:31797421-31797471	HAEpiC	amniotic membrane:	n/a
27	chr6:31797416-31797466	NH-A	brain:	n/a
28	chr6:31797416-31797466	AG09309	skin:	n/a
29	chr6:31797821-31797871	MCF-7	breast:	n/a
30	chr6:31797421-31797471	GM12892	blood:	n/a
31	chr6:31797421-31797471	IMR90	lung:	fetal
32	chr6:31797421-31797471	GM19239	blood:	n/a
33	chr6:31797421-31797471	HMEC	breast:	n/a
34	chr6:31797416-31797466	IMR90	lung:	fetal
35	chr6:31797821-31797871	AG10803	skin:	n/a
36	chr6:31797416-31797466	U87	brain:	n/a
37	chr6:31797416-31797466	HEEpiC	esophagus:	n/a
38	chr6:31797421-31797471	Caco-2	colon:	n/a
39	chr6:31797421-31797471	MCF10A-Er-Src	breast:	n/a
40	chr6:31797416-31797466	SKMC	muscle:	n/a
41	chr6:31797416-31797466	GM06990	blood:	n/a
42	chr6:31797821-31797871	GM12892	blood:	n/a
43	chr6:31797416-31797466	NHBE	bronchial:	n/a
44	chr6:31797416-31797466	AG04449	skin:	fetal
45	chr6:31797821-31797871	HIPEpiC	eye:	n/a
46	chr6:31797821-31797871	PANC-1	pancreas:	n/a
47	chr6:31797416-31797466	GM12878	blood:	n/a
48	chr6:31797821-31797871	ovcar-3	ovarian:	n/a
49	chr6:31797821-31797871	HNPCEpiC	eye:	n/a
50	chr6:31797416-31797466	A549	lung:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31796169..31798718-chr6:31855458..31858224,2	MCF-7	breast:
2	chr6:31797405..31799206-chr6:31828382..31830105,2	K562	blood:
3	chr16:89988437..89990274-chr6:31795215..31797917,2	MCF-7	breast:
4	chr6:31740578..31741288-chr6:31797704..31798376,4	MCF-7	breast:
5	chr6:31795326..31798240-chr6:31869248..31870828,2	K562	blood:
6	chr6:31706679..31708956-chr6:31795250..31798080,2	MCF-7	breast:
7	chr6:31648223..31648743-chr6:31797705..31798338,2	K562	blood:
8	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
9	chr6:31696240..31698841-chr6:31797761..31799583,2	MCF-7	breast:
10	chr6:31646374..31649912-chr6:31794618..31797680,6	MCF-7	breast:
11	chr6:31795638..31797726-chr6:32161977..32163708,2	K562	blood:
12	chr6:31795475..31798260-chr6:31864062..31867064,3	K562	blood:
13	chr6:31795540..31798054-chr6:31844082..31846588,3	K562	blood:
14	chr6:31695389..31697980-chr6:31796145..31797742,2	MCF-7	breast:
15	chr6:31508088..31512302-chr6:31792582..31797881,5	K562	blood:
16	chr6:31796727..31799560-chr6:31913553..31916544,2	MCF-7	breast:
17	chr6:31619174..31622035-chr6:31794476..31797735,3	MCF-7	breast:
18	chr15:50646997..50647926-chr6:31797241..31797843,2	Hela-S3	cervix:
19	chr6:31686048..31689889-chr6:31795401..31797897,4	MCF-7	breast:
20	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
21	chr6:31758502..31767561-chr6:31786193..31804196,52	MCF-7	breast:
22	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
23	chr6:31797792..31800637-chr6:32096282..32098134,2	K562	blood:
24	chr6:31586894..31588593-chr6:31796465..31799455,2	MCF-7	breast:
25	chr6:31740405..31741321-chr6:31797365..31798460,3	MCF-7	breast:
26	chr6:31795636..31798245-chr6:31918876..31922534,3	MCF-7	breast:
27	chr6:31696809..31697328-chr6:31797825..31798588,2	K562	blood:
28	chr6:31797497..31799469-chr6:31830033..31833133,3	MCF-7	breast:
29	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	HSPA1B	hsa-miR-15a-5p	chr6:31797698-31797719
2	HSPA1B	hsa-miR-16-5p	chr6:31797698-31797719
3	HSPA1B	hsa-miR-15a-5p	chr6:31797736-31797757
4	HSPA1B	hsa-miR-16-5p	chr6:31797736-31797757

Variant related genes	Relation type
C6orf48	TF binding region
C6orf48	CpG island
ENSG00000204396	chromatin interactions
ENSG00000204421	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000255152	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000204420	chromatin interactions
ENSG00000201555	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000213654	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000258947	chromatin interactions
ENSG00000204315	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204428	chromatin interactions

Extended variants
information (count: 30 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538280104	chr6:31797127-31797128	Weak transcription	Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
2	rs112626070	chr6:31797166-31797167	Weak transcription	Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
3	rs41312325	chr6:31797272-31797273	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	27 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536439406	chr6:31797287-31797288	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
5	rs113910452	chr6:31797329-31797330	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
6	rs371838772	chr6:31797406-31797407	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
7	rs377206432	chr6:31797416-31797417	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
8	rs56280220	chr6:31797422-31797423	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs35682610	chr6:31797437-31797438	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
10	rs370054194	chr6:31797455-31797456	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
11	rs576580373	chr6:31797459-31797460	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
12	rs200083915	chr6:31797502-31797503	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
13	rs537576552	chr6:31797555-31797556	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
14	rs376637337	chr6:31797582-31797583	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
15	rs539689	chr6:31797587-31797588	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
16	rs149254838	chr6:31797594-31797595	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
17	rs558798778	chr6:31797627-31797628	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
18	rs200684519	chr6:31797632-31797633	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
19	rs541068717	chr6:31797637-31797638	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
20	rs374210554	chr6:31797656-31797657	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
21	rs372841582	chr6:31797665-31797666	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
22	rs185921924	chr6:31797677-31797678	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
23	rs376092958	chr6:31797680-31797681	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
24	rs141231210	chr6:31797682-31797683	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
25	rs370072638	chr6:31797683-31797684	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
26	rs565503358	chr6:31797745-31797746	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region miRNA target site	24 gene(s)	Overlapped CNVs	n/a
27	rs146946127	chr6:31797747-31797748	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region miRNA target site	24 gene(s)	Overlapped CNVs	n/a
28	rs548786990	chr6:31797769-31797770	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
29	rs531028875	chr6:31797811-31797812	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
30	rs549822168	chr6:31797823-31797824	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31795000-31797400	Weak transcription	Fetal Heart	heart
2	chr6:31795200-31797400	Weak transcription	Fetal Brain Male	brain
3	chr6:31795800-31797200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:31795800-31797200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:31795800-31797200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:31795800-31797200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:31795800-31797200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:31795800-31797200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:31795800-31797200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr6:31795800-31797200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:31795800-31797200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:31795800-31797200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:31795800-31797200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:31795800-31797200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:31795800-31797200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr6:31795800-31797200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:31795800-31797200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:31795800-31797200	Weak transcription	Adipose Nuclei	Adipose
19	chr6:31795800-31797200	Weak transcription	Brain Angular Gyrus	brain
20	chr6:31795800-31797200	Weak transcription	Brain Anterior Caudate	brain
21	chr6:31795800-31797200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:31795800-31797200	Weak transcription	Brain Hippocampus Middle	brain
23	chr6:31795800-31797200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:31795800-31797200	Weak transcription	Brain Substantia Nigra	brain
25	chr6:31795800-31797200	Weak transcription	Colonic Mucosa	Colon
26	chr6:31795800-31797200	Weak transcription	Colon Smooth Muscle	Colon
27	chr6:31795800-31797200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:31795800-31797200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr6:31795800-31797200	Weak transcription	Fetal Lung	lung
30	chr6:31795800-31797200	Weak transcription	Placenta	Placenta
31	chr6:31795800-31797200	Weak transcription	Gastric	stomach
32	chr6:31795800-31797200	Weak transcription	Lung	lung
33	chr6:31795800-31797200	Weak transcription	Psoas Muscle	Psoas
34	chr6:31795800-31797200	Weak transcription	Right Atrium	heart
35	chr6:31795800-31797200	Weak transcription	Right Ventricle	heart
36	chr6:31795800-31797200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:31795800-31797200	Weak transcription	Thymus	Thymus
38	chr6:31795800-31797200	Weak transcription	A549	lung
39	chr6:31795800-31797200	Weak transcription	GM12878-XiMat	blood
40	chr6:31795800-31797200	Weak transcription	Hela-S3	cervix
41	chr6:31795800-31797200	Weak transcription	K562	blood
42	chr6:31795800-31797200	Weak transcription	NH-A	brain
43	chr6:31795800-31797200	Weak transcription	NHDF-Ad	bronchial
44	chr6:31795800-31797200	Weak transcription	NHEK	skin
45	chr6:31795800-31797200	Weak transcription	NHLF	lung
46	chr6:31795800-31797400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:31795800-31797400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:31795800-31797400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:31795800-31797400	Weak transcription	Primary B cells from cord blood	blood
50	chr6:31795800-31797400	Weak transcription	Primary B cells from peripheral blood	blood

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