Variant report

Variant	esv3386586
Chromosome Location	chr8:86553800-86576451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1124)
CpG islands
(count:1038)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:86572171-86572827	K562	blood:	n/a	n/a
2	ATF1	chr8:86563552-86563741	K562	blood:	n/a	n/a
3	BATF	chr8:86571642-86571818	GM12878	blood:	n/a	n/a
4	BATF	chr8:86557168-86557577	GM12878	blood:	n/a	n/a
5	BATF	chr8:86568243-86568407	GM12878	blood:	n/a	n/a
6	BATF	chr8:86575408-86576449	GM12878	blood:	n/a	n/a
7	BATF	chr8:86561630-86563893	GM12878	blood:	n/a	n/a
8	BATF	chr8:86559452-86559628	GM12878	blood:	n/a	n/a
9	BATF	chr8:86571412-86571576	GM12878	blood:	n/a	n/a
10	BATF	chr8:86565619-86566067	GM12878	blood:	n/a	n/a
11	BATF	chr8:86575381-86576452	GM12878	blood:	n/a	n/a
12	BATF	chr8:86571631-86571818	GM12878	blood:	n/a	n/a
13	BATF	chr8:86572676-86573086	GM12878	blood:	n/a	n/a
14	BATF	chr8:86559441-86559628	GM12878	blood:	n/a	n/a
15	BATF	chr8:86560587-86561595	GM12878	blood:	n/a	n/a
16	BATF	chr8:86568571-86569883	GM12878	blood:	n/a	n/a
17	BATF	chr8:86564638-86565178	GM12878	blood:	n/a	n/a
18	BATF	chr8:86564607-86565514	GM12878	blood:	n/a	n/a
19	BATF	chr8:86560585-86564464	GM12878	blood:	n/a	n/a
20	BATF	chr8:86557171-86557645	GM12878	blood:	n/a	n/a
21	BATF	chr8:86565192-86566244	GM12878	blood:	n/a	n/a
22	BATF	chr8:86568544-86569835	GM12878	blood:	n/a	n/a
23	BATF	chr8:86563900-86564422	GM12878	blood:	n/a	n/a
24	BATF	chr8:86556713-86557155	GM12878	blood:	n/a	n/a
25	BATF	chr8:86559222-86559386	GM12878	blood:	n/a	n/a
26	BATF	chr8:86556634-86557157	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:86573533-86573693	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:86566434-86566651	GM12878	blood:	n/a	chr8:86566633-86566646
29	BCL11A	chr8:86571624-86571904	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:86561626-86566123	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:86572144-86572407	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:86556317-86556493	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:86560578-86561581	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:86566453-86566637	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:86566696-86566856	GM12878	blood:	n/a	chr8:86566767-86566780
36	BCL11A	chr8:86562487-86563899	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:86561653-86562481	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:86559434-86559714	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:86557628-86557805	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:86575307-86576446	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:86575306-86576465	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:86559910-86560168	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:86563922-86564480	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:86560613-86561459	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:86568470-86569995	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:86564630-86565490	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:86557171-86557821	GM12878	blood:	n/a	chr8:86557185-86557194
48	BCL11A	chr8:86572077-86572356	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:86571642-86571878	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:86572960-86573188	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86564548-86564598	HUVEC	blood vessel:	n/a
2	chr8:86564548-86564598	HUVEC	blood vessel:	n/a
3	chr8:86560192-86560242	ECC-1	luminal epithelium:	n/a
4	chr8:86568078-86568128	Jurkat	blood:	n/a
5	chr8:86554026-86554076	GM12878	blood:	n/a
6	chr8:86556171-86556221	HRCEpiC	kidney:	n/a
7	chr8:86572367-86572417	NHBE	bronchial:	n/a
8	chr8:86554026-86554076	GM12892	blood:	n/a
9	chr8:86568078-86568128	HepG2	liver:	n/a
10	chr8:86573821-86573871	CMK	blood:	n/a
11	chr8:86568090-86568140	IMR90	lung:	fetal
12	chr8:86568078-86568128	HCT-116	colon:	n/a
13	chr8:86573821-86573871	AG09309	skin:	n/a
14	chr8:86556903-86556953	SK-N-SH_RA	brain:	n/a
15	chr8:86574469-86574519	ProgFib	skin:	n/a
16	chr8:86554026-86554076	AG09309	skin:	n/a
17	chr8:86556176-86556226	NHDF-neo	bronchial:	n/a
18	chr8:86564548-86564598	ProgFib	skin:	n/a
19	chr8:86554026-86554076	MCF10A-Er-Src	breast:	n/a
20	chr8:86556749-86556799	SK-N-MC	brain:	n/a
21	chr8:86556176-86556226	MCF-7	breast:	n/a
22	chr8:86568078-86568128	SKMC	muscle:	n/a
23	chr8:86574469-86574519	A549	lung:	n/a
24	chr8:86556176-86556226	HEK293	kidney:	embryo
25	chr8:86568078-86568128	NHBE	bronchial:	n/a
26	chr8:86554888-86554938	AoSMC	blood vessel:	n/a
27	chr8:86556903-86556953	U87	brain:	n/a
28	chr8:86574469-86574519	HCM	heart:	n/a
29	chr8:86568090-86568140	HMEC	breast:	n/a
30	chr8:86560192-86560242	AoSMC	blood vessel:	n/a
31	chr8:86568163-86568213	GM19239	blood:	n/a
32	chr8:86556171-86556221	MCF10A-Er-Src	breast:	n/a
33	chr8:86568163-86568213	GM12891	blood:	n/a
34	chr8:86572367-86572417	HEK293	kidney:	embryo
35	chr8:86567383-86567433	HEEpiC	esophagus:	n/a
36	chr8:86574449-86574499	HUVEC	blood vessel:	n/a
37	chr8:86573821-86573871	HepG2	liver:	n/a
38	chr8:86568163-86568213	SK-N-MC	brain:	n/a
39	chr8:86556749-86556799	AG10803	skin:	n/a
40	chr8:86556176-86556226	AoSMC	blood vessel:	n/a
41	chr8:86556176-86556226	HRPEpiC	eye:	n/a
42	chr8:86573821-86573871	AG10803	skin:	n/a
43	chr8:86556171-86556221	AG04450	lung:	fetal
44	chr8:86568163-86568213	PFSK-1	brain:	n/a
45	chr8:86554888-86554938	BJ	skin:	n/a
46	chr8:86556164-86556214	ProgFib	skin:	n/a
47	chr8:86568163-86568213	HepG2	liver:	n/a
48	chr8:86568090-86568140	AG04450	lung:	fetal
49	chr8:86554888-86554938	HCF	heart:	n/a
50	chr8:86568090-86568140	GM19239	blood:	n/a

No data

Variant related genes	Relation type
REXO1L3P	TF binding region
REXO1L1P	TF binding region
REXO1L8P	TF binding region
REXO1L3P	CpG island
REXO1L1P	CpG island
REXO1L8P	CpG island

Extended variants
information (count: 743 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532703629	chr8:86556704-86556705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368486442	chr8:86556721-86556722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552950738	chr8:86556736-86556737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563051443	chr8:86556749-86556750	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs531975183	chr8:86556757-86556758	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs548666774	chr8:86556763-86556764	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs568588322	chr8:86556778-86556779	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs370704832	chr8:86556781-86556782	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs75156223	chr8:86556793-86556794	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs183330176	chr8:86556797-86556798	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs539351905	chr8:86556802-86556803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556068836	chr8:86556841-86556842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375567138	chr8:86556844-86556845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187537836	chr8:86556849-86556850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs79909071	chr8:86556852-86556853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs555017635	chr8:86556869-86556870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572050663	chr8:86556885-86556886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs540982216	chr8:86556902-86556903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs563917395	chr8:86556903-86556904	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs192808569	chr8:86556904-86556905	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs5020115	chr8:86556923-86556924	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs546503277	chr8:86556931-86556932	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs563189554	chr8:86556968-86556969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531911305	chr8:86557002-86557003	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs548801351	chr8:86557026-86557027	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562169795	chr8:86557030-86557031	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs527772408	chr8:86557055-86557056	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7005473	chr8:86557059-86557060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570737542	chr8:86557086-86557087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs376707480	chr8:86557105-86557106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs549632508	chr8:86557115-86557116	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs367671125	chr8:86557126-86557127	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183353657	chr8:86557129-86557130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs7388011	chr8:86557131-86557132	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187845164	chr8:86557146-86557147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572245023	chr8:86557148-86557149	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs375127810	chr8:86557174-86557175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs142227636	chr8:86557193-86557194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs35972336	chr8:86557201-86557202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557868322	chr8:86557205-86557206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs6997260	chr8:86557206-86557207	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs35191773	chr8:86557218-86557219	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs6605623	chr8:86557220-86557221	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576816170	chr8:86557221-86557222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192870194	chr8:86557224-86557225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183795919	chr8:86557229-86557230	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs151184252	chr8:86557242-86557243	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs188120447	chr8:86557244-86557245	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs564621935	chr8:86557272-86557273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs533130006	chr8:86557322-86557323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86563400-86563800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr8:86563600-86563800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:86563800-86572200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:86564200-86564400	Weak transcription	Spleen	Spleen
5	chr8:86566200-86567800	Weak transcription	Pancreas	Pancrea
6	chr8:86567400-86567800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:86567400-86567800	Weak transcription	Spleen	Spleen
8	chr8:86567400-86568000	Weak transcription	Left Ventricle	heart
9	chr8:86567800-86568000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:86567800-86568200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:86567800-86568200	ZNF genes & repeats	Gastric	stomach
12	chr8:86567800-86568200	ZNF genes & repeats	Pancreas	Pancrea
13	chr8:86567800-86568200	ZNF genes & repeats	Spleen	Spleen
14	chr8:86568000-86568200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr8:86568000-86568200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:86568000-86568200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:86568000-86568200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr8:86568000-86568200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
19	chr8:86568000-86568200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr8:86568000-86568200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:86568000-86568200	ZNF genes & repeats	Esophagus	oesophagus
22	chr8:86568000-86568200	ZNF genes & repeats	Ovary	ovary
23	chr8:86568000-86568200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
24	chr8:86568000-86568200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
25	chr8:86568000-86568200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
26	chr8:86568200-86569600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:86568200-86569600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr8:86568200-86572000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr8:86568200-86572200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr8:86568200-86572200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:86568200-86572200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr8:86568400-86569800	Weak transcription	Ovary	ovary
33	chr8:86569600-86570000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:86569600-86570000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr8:86569800-86570000	Weak transcription	Left Ventricle	heart
36	chr8:86570000-86570600	Weak transcription	Ovary	ovary
37	chr8:86570000-86572000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr8:86570000-86572200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr8:86570200-86571600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:86570200-86572000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:86571800-86572000	Weak transcription	Left Ventricle	heart
42	chr8:86571800-86572200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr8:86572000-86572800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr8:86572000-86572800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
45	chr8:86572000-86572800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr8:86572000-86572800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
47	chr8:86572200-86572400	ZNF genes & repeats	Left Ventricle	heart
48	chr8:86572200-86572600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
49	chr8:86572200-86572600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:86572200-86572600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood

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