Variant report

Variant	nsv1017411
Chromosome Location	chr8:85536245-85596675
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	ARID3A	chr8:85538421-85538767	K562	blood:	n/a	n/a
2	ARID3A	chr8:85538348-85538838	HepG2	liver:	n/a	n/a
3	ATF2	chr8:85538406-85538701	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:85538319-85538721	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:85538051-85538743	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:85538378-85538685	K562	blood:	n/a	n/a
7	BRCA1	chr8:85538462-85538670	HepG2	liver:	n/a	chr8:85538617-85538624
8	CBX3	chr8:85538310-85538756	HCT-116	colon:	n/a	n/a
9	CBX3	chr8:85538256-85538849	HCT-116	colon:	n/a	n/a
10	CEBPB	chr8:85582525-85582816	A549	lung:	n/a	chr8:85582680-85582691
11	CEBPB	chr8:85588569-85588865	HepG2	liver:	n/a	chr8:85588668-85588679
12	CEBPB	chr8:85582523-85582840	HepG2	liver:	n/a	chr8:85582680-85582691
13	CEBPB	chr8:85538409-85538802	HepG2	liver:	n/a	chr8:85538664-85538677
14	CEBPB	chr8:85588098-85588856	A549	lung:	n/a	chr8:85588668-85588679
15	CEBPB	chr8:85569989-85570051	K562	blood:	n/a	n/a
16	CEBPB	chr8:85544647-85545320	IMR90	lung:	n/a	n/a
17	CEBPZ	chr8:85553098-85553381	HepG2	liver:	n/a	n/a
18	CHD2	chr8:85538505-85538628	HepG2	liver:	n/a	n/a
19	CREB1	chr8:85538399-85538638	A549	lung:	n/a	n/a
20	CTCF	chr8:85560580-85560730	GM12873	blood:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
21	CTCF	chr8:85538420-85538570	GM12873	blood:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
22	CTCF	chr8:85538342-85538881	A549	lung:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
23	CTCF	chr8:85560600-85560750	HPF	lung:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
24	CTCF	chr8:85560540-85560690	HUVEC	blood vessel:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
25	CTCF	chr8:85560520-85560670	A549	lung:	n/a	n/a
26	CTCF	chr8:85538367-85538774	HepG2	liver:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
27	CTCF	chr8:85560540-85560690	GM12872	blood:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
28	CTCF	chr8:85560497-85560834	K562	blood:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
29	CTCF	chr8:85538400-85538550	HA-sp	spinal cord:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
30	CTCF	chr8:85554699-85554790	GM10248	blood:	n/a	n/a
31	CTCF	chr8:85538381-85538751	Kidney_OC	kidney:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
32	CTCF	chr8:85538440-85538590	HPAF	blood vessel:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
33	CTCF	chr8:85538145-85539121	SK-N-SH	brain:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
34	CTCF	chr8:85560620-85560770	GM12873	blood:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
35	CTCF	chr8:85538440-85538590	GM12872	blood:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
36	CTCF	chr8:85560600-85560750	NB4	blood:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
37	CTCF	chr8:85538381-85538654	K562	blood:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
38	CTCF	chr8:85538138-85538240	GM20000	blood:	n/a	n/a
39	CTCF	chr8:85593673-85593729	GM13976	blood:	n/a	n/a
40	CTCF	chr8:85538420-85538570	NHLF	lung:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
41	CTCF	chr8:85538420-85538570	HRE	kidney:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
42	CTCF	chr8:85560336-85560388	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:85538357-85538783	Medullo	brain:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
44	CTCF	chr8:85538460-85538610	BE2_C	brain:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
45	CTCF	chr8:85560600-85560750	HRPEpiC	eye:	n/a	chr8:85560665-85560683 chr8:85560667-85560688
46	CTCF	chr8:85538420-85538570	GM12871	blood:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
47	CTCF	chr8:85538480-85538630	NHEK	skin:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
48	CTCF	chr8:85538369-85538756	LNCaP	prostate:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
49	CTCF	chr8:85538380-85538665	GM20000	blood:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519
50	CTCF	chr8:85538228-85538956	HCT-116	colon:	n/a	chr8:85538505-85538518 chr8:85538502-85538520 chr8:85538503-85538519

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:85538646-85538696	HEK293	kidney:	embryo
2	chr8:85538646-85538696	HRE	kidney:	n/a
3	chr8:85538646-85538696	HL-60	blood:	n/a
4	chr8:85538646-85538696	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:85538646-85538696	SK-N-SH_RA	brain:	n/a
6	chr8:85538646-85538696	ProgFib	skin:	n/a
7	chr8:85538646-85538696	HRCEpiC	kidney:	n/a
8	chr8:85538646-85538696	T-47D	breast:	n/a
9	chr8:85538646-85538696	SAEC	small airway:	n/a
10	chr8:85538646-85538696	HCF	heart:	n/a
11	chr8:85538646-85538696	CMK	blood:	n/a
12	chr8:85538646-85538696	HMEC	breast:	n/a
13	chr8:85538646-85538696	HCPEpiC	choroid plexus:	n/a
14	chr8:85538646-85538696	AoSMC	blood vessel:	n/a
15	chr8:85538646-85538696	HepG2	liver:	n/a
16	chr8:85538646-85538696	GM12878	blood:	n/a
17	chr8:85538646-85538696	HNPCEpiC	eye:	n/a
18	chr8:85538646-85538696	MCF-7	breast:	n/a
19	chr8:85538646-85538696	GM06990	blood:	n/a
20	chr8:85538646-85538696	AG09309	skin:	n/a
21	chr8:85538646-85538696	SK-N-SH	brain:	n/a
22	chr8:85538646-85538696	SKMC	muscle:	n/a
23	chr8:85538646-85538696	PANC-1	pancreas:	n/a
24	chr8:85538646-85538696	IMR90	lung:	fetal
25	chr8:85538646-85538696	HIPEpiC	eye:	n/a
26	chr8:85538646-85538696	MCF10A-Er-Src	breast:	n/a
27	chr8:85538646-85538696	NHDF-neo	bronchial:	n/a
28	chr8:85538646-85538696	HAEpiC	amniotic membrane:	n/a
29	chr8:85538646-85538696	K562	blood:	n/a
30	chr8:85538646-85538696	ECC-1	luminal epithelium:	n/a
31	chr8:85538646-85538696	AG04450	lung:	fetal
32	chr8:85538646-85538696	RPTEC	kidney:	n/a
33	chr8:85538646-85538696	PrEC	prostate:	n/a
34	chr8:85538646-85538696	HEEpiC	esophagus:	n/a
35	chr8:85538646-85538696	Hepatocyte	liver:	n/a
36	chr8:85538646-85538696	U87	brain:	n/a
37	chr8:85538646-85538696	LNCaP	prostate:	n/a
38	chr8:85538646-85538696	HUVEC	blood vessel:	n/a
39	chr8:85538646-85538696	Hela-S3	cervix:	n/a
40	chr8:85538646-85538696	AG09319	gingival:	n/a
41	chr8:85538646-85538696	A549	lung:	n/a
42	chr8:85538646-85538696	NT2-D1	testis:	n/a
43	chr8:85538646-85538696	GM19239	blood:	n/a
44	chr8:85538646-85538696	SK-N-MC	brain:	n/a
45	chr8:85538646-85538696	AG10803	skin:	n/a
46	chr8:85538646-85538696	NHBE	bronchial:	n/a
47	chr8:85538646-85538696	Jurkat	blood:	n/a
48	chr8:85538646-85538696	H1-hESC	embryonic stem cell:	embryo
49	chr8:85538646-85538696	GM12891	blood:	n/a
50	chr8:85538646-85538696	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:85542893..85545480-chr8:86287576..86290240,2	MCF-7	breast:
2	chr8:85560177..85561443-chr8:85966429..85967093,4	MCF-7	breast:
3	chr8:85533470..85536280-chr8:85567297..85568905,2	K562	blood:
4	chr17:61159360..61159868-chr8:85538366..85539003,2	MCF-7	breast:
5	chr8:85538381..85538975-chr8:86059742..86060294,2	MCF-7	breast:
6	chr8:85564527..85566559-chr8:85570080..85572142,2	K562	blood:
7	chr8:85533470..85536280-chr8:85567297..85568905,2	K562	blood:
8	chr8:85559754..85561199-chr8:85943458..85945114,8	MCF-7	breast:
9	chr8:85538123..85539046-chr8:85966580..85967573,4	MCF-7	breast:
10	chr8:85538196..85539101-chr8:85944207..85944819,2	MCF-7	breast:
11	chr8:85538159..85539035-chr8:85943804..85944923,5	MCF-7	breast:
12	chr8:85538135..85538922-chr8:86202235..86203001,3	MCF-7	breast:
13	chr8:85564527..85566559-chr8:85570080..85572142,2	K562	blood:
14	chr8:85534205..85536062-chr8:85543701..85545825,2	MCF-7	breast:
15	chr8:85560187..85560882-chr8:85966636..85967302,2	MCF-7	breast:
16	chr8:85538325..85539130-chr8:85944090..85944900,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRCC1-3	chr8:85591033-85592077	NONHSAT127504

Variant related genes	Relation type
ENSG00000253137	TF binding region
RNU6-1040P	TF binding region
ENSG00000253137	CpG island
RNU6-1040P	CpG island

Extended variants
information (count: 760 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553966938	chr8:85536800-85536801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529196326	chr8:85536837-85536838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369126749	chr8:85536936-85536937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149790493	chr8:85536937-85536938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554201526	chr8:85537008-85537009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34971448	chr8:85537031-85537032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528248462	chr8:85537038-85537039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572747900	chr8:85537085-85537086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567567665	chr8:85537126-85537127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570600914	chr8:85537168-85537169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188077010	chr8:85537248-85537249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536593542	chr8:85537252-85537253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181037013	chr8:85537255-85537256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62530161	chr8:85537483-85537484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555181126	chr8:85537555-85537556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536171327	chr8:85537569-85537570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78605411	chr8:85537649-85537650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535114878	chr8:85537664-85537665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572634856	chr8:85537667-85537668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535766092	chr8:85537706-85537707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557672686	chr8:85537710-85537711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187158802	chr8:85537764-85537765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190828163	chr8:85537791-85537792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145768012	chr8:85537828-85537829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141499942	chr8:85537916-85537917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182142937	chr8:85537932-85537933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573529404	chr8:85537947-85537948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17788618	chr8:85537976-85537977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs386727367	chr8:85537978-85537979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4302839	chr8:85537979-85537980	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544798602	chr8:85538074-85538075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564699087	chr8:85538121-85538122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533268374	chr8:85538149-85538150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549837598	chr8:85538153-85538154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570064231	chr8:85538209-85538210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529256930	chr8:85538217-85538218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549691520	chr8:85538274-85538275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566240804	chr8:85538283-85538284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186815804	chr8:85538298-85538299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147036911	chr8:85538321-85538322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571834913	chr8:85538340-85538341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190698764	chr8:85538403-85538404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139879371	chr8:85538419-85538420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556755577	chr8:85538443-85538444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573612930	chr8:85538461-85538462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542247409	chr8:85538485-85538486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35373915	chr8:85538497-85538498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553277922	chr8:85538539-85538540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572812132	chr8:85538548-85538549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544871899	chr8:85538549-85538550	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85536800-85537200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:85537200-85537600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:85537600-85538200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:85537600-85538400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr8:85537800-85538600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:85538000-85538200	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:85538000-85538800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:85539000-85539400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:85542000-85543200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:85542400-85542600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:85542400-85542600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr8:85542400-85542600	Enhancers	HSMM	muscle
13	chr8:85542400-85543000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:85542400-85543000	Enhancers	NHDF-Ad	bronchial
15	chr8:85542400-85543000	Enhancers	NHLF	lung
16	chr8:85542600-85542800	Enhancers	Osteobl	bone
17	chr8:85542600-85543000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:85542600-85543000	Enhancers	NH-A	brain
19	chr8:85542600-85544400	Weak transcription	HSMM	muscle
20	chr8:85542800-85544600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:85543000-85544200	Weak transcription	NHDF-Ad	bronchial
22	chr8:85543000-85544400	Weak transcription	NHLF	lung
23	chr8:85543000-85544600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:85543000-85544600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr8:85543000-85544600	Weak transcription	NH-A	brain
26	chr8:85543200-85544200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:85544200-85544800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:85544200-85546000	Enhancers	NHDF-Ad	bronchial
29	chr8:85544200-85546200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:85544400-85545600	Enhancers	HSMM	muscle
31	chr8:85544400-85545600	Enhancers	NHLF	lung
32	chr8:85544400-85545800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:85544600-85544800	Weak transcription	Osteobl	bone
34	chr8:85544600-85545400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr8:85544600-85545600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:85544600-85545600	Enhancers	HSMMtube	muscle
37	chr8:85544600-85546000	Enhancers	Fetal Heart	heart
38	chr8:85544600-85546000	Enhancers	NH-A	brain
39	chr8:85544600-85546200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:85544600-85546200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:85544800-85545800	Enhancers	Osteobl	bone
42	chr8:85552000-85556400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:85560200-85560600	Enhancers	Fetal Brain Male	brain
44	chr8:85564800-85565800	Enhancers	Colon Smooth Muscle	Colon
45	chr8:85565800-85566600	Weak transcription	Colon Smooth Muscle	Colon
46	chr8:85566800-85567000	Enhancers	Colon Smooth Muscle	Colon
47	chr8:85571000-85571400	Active TSS	Brain Anterior Caudate	brain
48	chr8:85574000-85574600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:85574200-85574600	Enhancers	NH-A	brain
50	chr8:85580800-85583400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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