Variant report

Variant	esv3380616
Chromosome Location	chr8:143958651-143996737
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	BATF	chr8:143987622-143987828	GM12878	blood:	n/a	chr8:143987764-143987775
2	BHLHE40	chr8:143959425-143959448	K562	blood:	n/a	n/a
3	BHLHE40	chr8:143975344-143975622	K562	blood:	n/a	n/a
4	BHLHE40	chr8:143975332-143975632	HepG2	liver:	n/a	n/a
5	CBX3	chr8:143993340-143993685	K562	blood:	n/a	n/a
6	CEBPB	chr8:143975315-143975613	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr8:143968205-143968520	K562	blood:	n/a	n/a
8	CTCF	chr8:143994563-143994638	GM12892	blood:	n/a	n/a
9	CTCF	chr8:143994599-143994742	GM10248	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
10	CTCF	chr8:143994622-143994697	Hela-S3	cervix:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
11	CTCF	chr8:143987000-143987150	GM12875	blood:	n/a	n/a
12	CTCF	chr8:143994581-143994712	K562	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
13	CTCF	chr8:143988720-143988870	HCT-116	colon:	n/a	n/a
14	CTCF	chr8:143994568-143994734	GM12891	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
15	CTCF	chr8:143961678-143961759	GM20000	blood:	n/a	n/a
16	CTCF	chr8:143994720-143994870	GM12871	blood:	n/a	n/a
17	CTCF	chr8:143994586-143994696	GM19238	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
18	CTCF	chr8:143968885-143968916	K562	blood:	n/a	n/a
19	CUX1	chr8:143977763-143977837	K562	blood:	n/a	n/a
20	EBF1	chr8:143979537-143979979	GM12878	blood:	n/a	n/a
21	EBF1	chr8:143989032-143989208	GM12878	blood:	n/a	n/a
22	EGR1	chr8:143993819-143994054	K562	blood:	n/a	chr8:143993918-143993932 chr8:143993919-143993932 chr8:143993920-143993929 chr8:143993925-143993938 chr8:143993919-143993932 chr8:143993919-143993932 chr8:143993919-143993929 chr8:143993914-143993936 chr8:143993923-143993933 chr8:143993877-143993887 chr8:143993918-143993933 chr8:143993919-143993932
23	EGR1	chr8:143993744-143994024	K562	blood:	n/a	chr8:143993918-143993932 chr8:143993919-143993932 chr8:143993920-143993929 chr8:143993925-143993938 chr8:143993919-143993932 chr8:143993919-143993932 chr8:143993919-143993929 chr8:143993914-143993936 chr8:143993923-143993933 chr8:143993877-143993887 chr8:143993918-143993933 chr8:143993919-143993932
24	ELF1	chr8:143993382-143993601	HepG2	liver:	n/a	chr8:143993487-143993500
25	ELF1	chr8:143993285-143993676	K562	blood:	n/a	chr8:143993487-143993500
26	ELF1	chr8:143993227-143993853	MCF-7	breast:	n/a	chr8:143993487-143993500
27	ELK1	chr8:143983813-143983816	Hela-S3	cervix:	n/a	n/a
28	EP300	chr8:143979443-143980098	GM12878	blood:	n/a	n/a
29	EP300	chr8:143987188-143987251	K562	blood:	n/a	n/a
30	FOSL2	chr8:143979468-143980152	HepG2	liver:	n/a	n/a
31	FOXA2	chr8:143979465-143980049	A549	lung:	n/a	n/a
32	FOXP2	chr8:143983504-143983917	SK-N-MC	brain:	n/a	n/a
33	GABPA	chr8:143979778-143980075	Hela-S3	cervix:	n/a	n/a
34	GABPA	chr8:143979480-143979775	Hela-S3	cervix:	n/a	n/a
35	GATA1	chr8:143975138-143975670	PBDE	blood:	n/a	n/a
36	GATA3	chr8:143981134-143981524	T-47D	breast:	n/a	n/a
37	HCFC1	chr8:143993429-143993611	K562	blood:	n/a	n/a
38	HEY1	chr8:143979414-143980147	K562	blood:	n/a	n/a
39	IRF4	chr8:143979516-143979822	GM12878	blood:	n/a	n/a
40	IRF4	chr8:143979391-143980186	GM12878	blood:	n/a	n/a
41	JUN	chr8:143984574-143984774	K562	blood:	n/a	n/a
42	JUND	chr8:143979829-143980089	HepG2	liver:	n/a	n/a
43	JUND	chr8:143991527-143991650	K562	blood:	n/a	n/a
44	MAFK	chr8:143983704-143983817	HepG2	liver:	n/a	chr8:143983728-143983743
45	MAFK	chr8:143983696-143983813	HepG2	liver:	n/a	chr8:143983728-143983743
46	MAX	chr8:143959375-143959454	HepG2	liver:	n/a	chr8:143959383-143959393
47	MAX	chr8:143993376-143993691	K562	blood:	n/a	n/a
48	MAX	chr8:143959320-143959583	A549	lung:	n/a	chr8:143959371-143959381 chr8:143959383-143959393
49	MAX	chr8:143993493-143993519	NB4	blood:	n/a	n/a
50	MAX	chr8:143993312-143994031	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:143961145-143961195	SKMC	muscle:	n/a
2	chr8:143961145-143961195	SKMC	muscle:	n/a
3	chr8:143995000-143995050	NHDF-neo	bronchial:	n/a
4	chr8:143992652-143992702	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:143961341-143961391	GM06990	blood:	n/a
6	chr8:143992652-143992702	H1-hESC	embryonic stem cell:	embryo
7	chr8:143960794-143960844	NHDF-neo	bronchial:	n/a
8	chr8:143961141-143961191	NH-A	brain:	n/a
9	chr8:143961141-143961191	ProgFib	skin:	n/a
10	chr8:143961145-143961195	T-47D	breast:	n/a
11	chr8:143961145-143961195	AG04450	lung:	fetal
12	chr8:143961341-143961391	H1-hESC	embryonic stem cell:	embryo
13	chr8:143960794-143960844	PFSK-1	brain:	n/a
14	chr8:143961141-143961191	GM12892	blood:	n/a
15	chr8:143961391-143961441	K562	blood:	n/a
16	chr8:143961145-143961195	BE2_C	brain:	n/a
17	chr8:143992652-143992702	NH-A	brain:	n/a
18	chr8:143995000-143995050	A549	lung:	n/a
19	chr8:143960794-143960844	HRPEpiC	eye:	n/a
20	chr8:143992652-143992702	GM12878	blood:	n/a
21	chr8:143961341-143961391	HL-60	blood:	n/a
22	chr8:143961391-143961441	GM12878	blood:	n/a
23	chr8:143961145-143961195	HepG2	liver:	n/a
24	chr8:143961141-143961191	HEEpiC	esophagus:	n/a
25	chr8:143995000-143995050	HepG2	liver:	n/a
26	chr8:143960794-143960844	HRCEpiC	kidney:	n/a
27	chr8:143961341-143961391	HCPEpiC	choroid plexus:	n/a
28	chr8:143960794-143960844	HEEpiC	esophagus:	n/a
29	chr8:143961391-143961441	HL-60	blood:	n/a
30	chr8:143961341-143961391	GM12891	blood:	n/a
31	chr8:143961141-143961191	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:143961391-143961441	HRCEpiC	kidney:	n/a
33	chr8:143961141-143961191	HCF	heart:	n/a
34	chr8:143961291-143961341	GM12891	blood:	n/a
35	chr8:143961391-143961441	HEK293	kidney:	embryo
36	chr8:143992652-143992702	HMEC	breast:	n/a
37	chr8:143995000-143995050	ovcar-3	ovarian:	n/a
38	chr8:143961145-143961195	BJ	skin:	n/a
39	chr8:143960794-143960844	HRE	kidney:	n/a
40	chr8:143961391-143961441	AG09319	gingival:	n/a
41	chr8:143961141-143961191	GM06990	blood:	n/a
42	chr8:143960794-143960844	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:143992652-143992702	HCT-116	colon:	n/a
44	chr8:143995000-143995050	HRPEpiC	eye:	n/a
45	chr8:143961145-143961195	A549	lung:	n/a
46	chr8:143961291-143961341	HMEC	breast:	n/a
47	chr8:143961291-143961341	K562	blood:	n/a
48	chr8:143961341-143961391	NHDF-neo	bronchial:	n/a
49	chr8:143992652-143992702	AoSMC	blood vessel:	n/a
50	chr8:143961341-143961391	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:143956006..143958994-chr8:144119486..144121629,2	MCF-7	breast:
2	chr8:143928685..143930379-chr8:143986753..143989580,2	K562	blood:
3	chr8:143982631..143984699-chr8:143987404..143990195,2	K562	blood:
4	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:
5	chr8:143982631..143984699-chr8:143987404..143990195,2	K562	blood:
6	chr8:143970505..143972946-chr8:143997611..144000246,2	MCF-7	breast:
7	chr8:143955912..143957781-chr8:143987320..143989042,2	MCF-7	breast:
8	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LY6E-4	chr8:143959812-143960330	NONHSAT129503

Variant related genes	Relation type
CYP11B1	TF binding region
CYP11B1	CpG island
ENSG00000179142	chromatin interactions
ENSG00000160882	chromatin interactions
ENSG00000177335	chromatin interactions

Extended variants
information (count: 1817 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61751147	chr8:143958660-143958661	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551914122	chr8:143958678-143958679	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs61751146	chr8:143958680-143958681	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs61751145	chr8:143958688-143958689	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528027778	chr8:143958695-143958696	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs61751144	chr8:143958696-143958697	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566959856	chr8:143958697-143958698	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537814960	chr8:143958706-143958707	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61751143	chr8:143958729-143958730	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs61751142	chr8:143958731-143958732	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568550441	chr8:143958781-143958782	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554048672	chr8:143958784-143958785	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572264268	chr8:143958786-143958787	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542970038	chr8:143958795-143958796	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574312809	chr8:143958798-143958799	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191976842	chr8:143958803-143958804	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146706300	chr8:143958804-143958805	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185102236	chr8:143958805-143958806	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373713714	chr8:143958820-143958821	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35378570	chr8:143958843-143958844	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7814006	chr8:143958911-143958912	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs139090252	chr8:143958917-143958918	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs66470473	chr8:143958930-143958931	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188817798	chr8:143958940-143958941	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7814020	chr8:143958941-143958942	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113143466	chr8:143958969-143958970	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368921558	chr8:143959021-143959022	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs560343228	chr8:143959053-143959054	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs80101721	chr8:143959067-143959068	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs71513667	chr8:143959076-143959077	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs527865805	chr8:143959113-143959114	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs549281636	chr8:143959121-143959122	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs561219388	chr8:143959144-143959145	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs374195902	chr8:143959165-143959166	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs75717953	chr8:143959174-143959175	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs368303228	chr8:143959176-143959177	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs9657020	chr8:143959188-143959189	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs547491853	chr8:143959205-143959206	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs11775687	chr8:143959219-143959220	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs536414549	chr8:143959241-143959242	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs7818826	chr8:143959250-143959251	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs144897910	chr8:143959257-143959258	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs368740606	chr8:143959262-143959263	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs568561435	chr8:143959270-143959271	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs9657021	chr8:143959272-143959273	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs79102214	chr8:143959279-143959280	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs7818953	chr8:143959289-143959290	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545132363	chr8:143959296-143959297	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs12542799	chr8:143959311-143959312	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs75079139	chr8:143959332-143959333	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Gastric cancer	24379144	CNVD
Sezary syndrome	18413736	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Colorectal cancer	16272173	CNVD
Glioma	17123091	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Esophageal squamous carcinoma	17470683	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Astrocytoma	22246337	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21806811	CNVD
Chylomicronemia	22008945	CNVD
Heart disease	21282601	CNVD
Chordoma	21602918	CNVD
Neuroblastoma	18923191	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	16397240	CNVD
Colorectal cancer	19455253	CNVD
Myxofibrosarcoma	16751306	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Oral cancer	22144094	CNVD
XY gonadal dysgenesis	20685758	CNVD
Cancer	20581869	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Pancreatic cancer	21811587	CNVD
Prostate cancer	22341455	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:143956600-143960800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:143958000-143959000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
3	chr8:143959000-143961000	Transcr. at gene 5' and 3'	Fetal Adrenal Gland	Adrenal Gland
4	chr8:143959200-143960000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:143960800-143961200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:143961000-143961200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
7	chr8:143961000-143961400	Enhancers	Spleen	Spleen
8	chr8:143961200-143961400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
9	chr8:143961200-143969800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:143961400-143961800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr8:143969800-143970400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:143970400-143992600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:143975000-143975600	Enhancers	Duodenum Mucosa	Duodenum
14	chr8:143975800-143976000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:143976000-143977400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:143977400-143977600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:143979000-143979600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:143988000-143989200	Enhancers	HepG2	liver
19	chr8:143991200-143991600	Enhancers	Primary T cells fromperipheralblood	blood
20	chr8:143991200-143991600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr8:143991200-143992200	Enhancers	Spleen	Spleen
22	chr8:143991400-143992000	Enhancers	Primary B cells from peripheral blood	blood
23	chr8:143992200-143993200	Weak transcription	Spleen	Spleen
24	chr8:143992600-143993400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:143993200-143993400	Enhancers	Spleen	Spleen
26	chr8:143993400-143993600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr8:143993400-143993600	Genic enhancers	Spleen	Spleen
28	chr8:143993400-143993800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:143993600-143995000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr8:143993600-143995200	Weak transcription	Spleen	Spleen
31	chr8:143993800-143994200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:143994200-144003200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:143994400-143994600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:143994800-143995400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr8:143995000-143995400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr8:143995200-143996000	Enhancers	Spleen	Spleen
37	chr8:143995400-143995600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr8:143996000-144003000	Weak transcription	Spleen	Spleen

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