Variant report

Variant	nsv1032389
Chromosome Location	chr8:111250159-111445816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111370803-111370846	K562	blood:	n/a	n/a
2	BACH1	chr8:111361264-111361282	K562	blood:	n/a	n/a
3	BATF	chr8:111380529-111380748	GM12878	blood:	n/a	n/a
4	BATF	chr8:111380515-111380775	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:111348693-111348897	A549	lung:	n/a	n/a
6	CEBPB	chr8:111407564-111407694	HepG2	liver:	n/a	chr8:111407634-111407645
7	CEBPB	chr8:111392636-111392756	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:111346863-111346939	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:111326111-111326430	HepG2	liver:	n/a	chr8:111326272-111326283
10	CEBPB	chr8:111326135-111326438	IMR90	lung:	n/a	chr8:111326272-111326283
11	CEBPB	chr8:111311633-111311681	A549	lung:	n/a	chr8:111311652-111311663
12	CEBPB	chr8:111311551-111311683	H1-hESC	embryonic stem cell:	n/a	chr8:111311652-111311663
13	CEBPB	chr8:111311571-111311766	HepG2	liver:	n/a	chr8:111311652-111311663
14	CEBPB	chr8:111271067-111271189	HepG2	liver:	n/a	chr8:111271123-111271134
15	CEBPB	chr8:111326176-111326371	K562	blood:	n/a	chr8:111326272-111326283
16	CEBPB	chr8:111326108-111326428	A549	lung:	n/a	chr8:111326272-111326283
17	CEBPB	chr8:111407057-111407265	HepG2	liver:	n/a	chr8:111407125-111407136
18	CEBPB	chr8:111425593-111425738	A549	lung:	n/a	n/a
19	CEBPB	chr8:111407619-111407631	K562	blood:	n/a	n/a
20	CEBPB	chr8:111407025-111407692	A549	lung:	n/a	chr8:111407634-111407645 chr8:111407125-111407136
21	CREB1	chr8:111380421-111380812	GM12878	blood:	n/a	n/a
22	CTCF	chr8:111299840-111299990	HPF	lung:	n/a	n/a
23	CTCF	chr8:111253015-111253075	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:111365520-111365670	BE2_C	brain:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
25	CTCF	chr8:111365480-111365630	HPAF	blood vessel:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
26	CTCF	chr8:111367120-111367270	BE2_C	brain:	n/a	n/a
27	CTCF	chr8:111367120-111367270	GM12864	blood:	n/a	n/a
28	CTCF	chr8:111367033-111367346	GM12878	blood:	n/a	n/a
29	CTCF	chr8:111345480-111345630	GM06990	blood:	n/a	n/a
30	CTCF	chr8:111367141-111367222	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:111303274-111303371	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:111270447-111270543	ProgFib	skin:	n/a	n/a
33	CTCF	chr8:111365500-111365650	MCF-7	breast:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
34	CTCF	chr8:111365461-111365827	MCF-7	breast:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
35	CTCF	chr8:111365500-111365650	AG10803	skin:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
36	CTCF	chr8:111365531-111365638	MCF-7	breast:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
37	CTCF	chr8:111367094-111367268	Medullo	brain:	n/a	n/a
38	CTCF	chr8:111365960-111366110	BE2_C	brain:	n/a	n/a
39	CTCF	chr8:111365480-111365630	RPTEC	kidney:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
40	CTCF	chr8:111365420-111365570	HAc	cerebellar:	n/a	n/a
41	CTCF	chr8:111365880-111366030	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:111365500-111365650	AG09319	gingival:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
43	CTCF	chr8:111367146-111367219	NHEK	skin:	n/a	n/a
44	CTCF	chr8:111367158-111367209	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:111419195-111419237	GM13976	blood:	n/a	n/a
46	CTCF	chr8:111430903-111430914	GM13976	blood:	n/a	n/a
47	CTCF	chr8:111365400-111365550	HVMF	connective:	n/a	n/a
48	CTCF	chr8:111367102-111367253	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:111367040-111367190	GM12874	blood:	n/a	n/a
50	CTCF	chr8:111367060-111367210	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111342449-111342499	HCM	heart:	n/a
2	chr8:111342449-111342499	K562	blood:	n/a
3	chr8:111342449-111342499	HMEC	breast:	n/a
4	chr8:111342449-111342499	LNCaP	prostate:	n/a
5	chr8:111342449-111342499	T-47D	breast:	n/a
6	chr8:111342449-111342499	SK-N-MC	brain:	n/a
7	chr8:111342449-111342499	IMR90	lung:	fetal
8	chr8:111342449-111342499	Caco-2	colon:	n/a
9	chr8:111342449-111342499	HIPEpiC	eye:	n/a
10	chr8:111342449-111342499	MCF-7	breast:	n/a
11	chr8:111342449-111342499	HepG2	liver:	n/a
12	chr8:111342449-111342499	SAEC	small airway:	n/a
13	chr8:111342449-111342499	HAEpiC	amniotic membrane:	n/a
14	chr8:111342449-111342499	HEEpiC	esophagus:	n/a
15	chr8:111342449-111342499	H1-hESC	embryonic stem cell:	embryo
16	chr8:111342449-111342499	HCT-116	colon:	n/a
17	chr8:111342449-111342499	SK-N-SH	brain:	n/a
18	chr8:111342449-111342499	HRE	kidney:	n/a
19	chr8:111342449-111342499	GM06990	blood:	n/a
20	chr8:111342449-111342499	Hela-S3	cervix:	n/a
21	chr8:111342449-111342499	PFSK-1	brain:	n/a
22	chr8:111342449-111342499	CMK	blood:	n/a
23	chr8:111342449-111342499	AG04449	skin:	fetal
24	chr8:111342449-111342499	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:111342449-111342499	NT2-D1	testis:	n/a
26	chr8:111342449-111342499	GM19239	blood:	n/a
27	chr8:111342449-111342499	AG04450	lung:	fetal
28	chr8:111342449-111342499	ovcar-3	ovarian:	n/a
29	chr8:111342449-111342499	HCPEpiC	choroid plexus:	n/a
30	chr8:111342449-111342499	HCF	heart:	n/a
31	chr8:111342449-111342499	AoSMC	blood vessel:	n/a
32	chr8:111342449-111342499	NHDF-neo	bronchial:	n/a
33	chr8:111342449-111342499	GM12891	blood:	n/a
34	chr8:111342449-111342499	GM12878	blood:	n/a
35	chr8:111342449-111342499	Jurkat	blood:	n/a
36	chr8:111342449-111342499	HNPCEpiC	eye:	n/a
37	chr8:111342449-111342499	HRPEpiC	eye:	n/a
38	chr8:111342449-111342499	GM12892	blood:	n/a
39	chr8:111342449-111342499	BE2_C	brain:	n/a
40	chr8:111342449-111342499	HL-60	blood:	n/a
41	chr8:111342449-111342499	NH-A	brain:	n/a
42	chr8:111342449-111342499	ECC-1	luminal epithelium:	n/a
43	chr8:111342449-111342499	A549	lung:	n/a
44	chr8:111342449-111342499	SK-N-SH_RA	brain:	n/a
45	chr8:111342449-111342499	AG09309	skin:	n/a
46	chr8:111342449-111342499	RPTEC	kidney:	n/a
47	chr8:111342449-111342499	U87	brain:	n/a
48	chr8:111342449-111342499	BJ	skin:	n/a
49	chr8:111342449-111342499	NB4	blood:	n/a
50	chr8:111342449-111342499	Hepatocyte	liver:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:111426432..111429583-chr8:111430116..111432569,3	MCF-7	breast:
2	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:
3	chr8:111426582..111428380-chr8:111435676..111438119,2	K562	blood:
4	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
5	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
6	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:
7	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
8	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
9	chr8:111246550..111249022-chr8:111251445..111253092,2	MCF-7	breast:
10	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
11	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
12	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
13	chr8:111444766..111447245-chr8:111451075..111453827,2	K562	blood:
14	chr8:100177691..100178432-chr8:111254768..111255288,2	MCF-7	breast:
15	chr7:157675743..157676555-chr8:111424512..111425012,2	Hela-S3	cervix:
16	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
17	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
18	chr8:111426582..111428380-chr8:111435676..111438119,2	K562	blood:
19	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
20	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:
21	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
22	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:
23	chr8:111100909..111103732-chr8:111408499..111410564,2	K562	blood:
24	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
25	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
26	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
27	chr8:111426432..111429583-chr8:111430116..111432569,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-1	chr8:111356682-111356824	ENSG00000253956
2	lnc-KCNV1-1	chr8:111361774-111361836	ENSG00000253956
3	lnc-KCNV1-1	chr8:111346972-111347538	ENSG00000253956

No data

Variant related genes	Relation type
ENSG00000253956	TF binding region
ENSG00000253956	CpG island

Extended variants
information (count: 3416 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3416 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368021939	chr8:111250165-111250166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545724888	chr8:111250184-111250185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562558690	chr8:111250247-111250248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564977155	chr8:111250308-111250309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371841786	chr8:111250311-111250312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541948254	chr8:111250326-111250327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561638766	chr8:111250344-111250345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370258479	chr8:111250350-111250351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144673137	chr8:111250362-111250363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4610716	chr8:111250380-111250381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4610717	chr8:111250382-111250383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548053470	chr8:111250449-111250450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200812054	chr8:111250472-111250473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375828188	chr8:111250520-111250521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148702807	chr8:111250615-111250616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142208596	chr8:111250634-111250635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569920111	chr8:111250671-111250672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181737172	chr8:111250727-111250728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549083504	chr8:111250734-111250735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146736296	chr8:111250759-111250760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534738179	chr8:111250772-111250773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527422321	chr8:111250807-111250808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554029302	chr8:111250812-111250813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139266909	chr8:111250817-111250818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539726816	chr8:111250848-111250849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556345073	chr8:111250878-111250879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576326195	chr8:111250885-111250886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144052164	chr8:111250897-111250898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368514344	chr8:111250955-111250956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146439549	chr8:111251000-111251001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536743564	chr8:111251005-111251006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74867575	chr8:111251084-111251085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140716148	chr8:111251110-111251111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529719656	chr8:111251131-111251132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571984737	chr8:111251169-111251170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540712062	chr8:111251239-111251240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187164797	chr8:111251248-111251249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568574467	chr8:111251289-111251290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533413728	chr8:111251305-111251306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550051276	chr8:111251322-111251323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368195948	chr8:111251354-111251355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563508731	chr8:111251392-111251393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529481741	chr8:111251461-111251462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549046388	chr8:111251463-111251464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566085787	chr8:111251483-111251484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528474815	chr8:111251491-111251492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551443486	chr8:111251498-111251499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571615891	chr8:111251536-111251537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374389595	chr8:111251556-111251557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377277179	chr8:111251610-111251611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
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
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111225600-111256400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:111256400-111258200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:111258200-111273000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:111268400-111268600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:111268600-111270000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:111270000-111270400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:111270000-111270600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr8:111272000-111272200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:111299600-111300000	Enhancers	Fetal Intestine Large	intestine
10	chr8:111301200-111301600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:111301200-111301800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr8:111301400-111301800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:111302400-111304800	Enhancers	Fetal Brain Male	brain
14	chr8:111303200-111306200	Enhancers	Fetal Brain Female	brain
15	chr8:111303800-111304000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:111304400-111305400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:111304800-111305200	Weak transcription	Fetal Brain Male	brain
18	chr8:111305200-111306000	Enhancers	Fetal Brain Male	brain
19	chr8:111305400-111305800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:111310800-111311000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:111311000-111322400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:111321800-111324000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:111322200-111324200	Enhancers	HMEC	breast
24	chr8:111322400-111323000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:111322400-111324200	Enhancers	NHEK	skin
26	chr8:111322600-111324000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:111323000-111323400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:111323400-111325000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:111324200-111334000	Weak transcription	HMEC	breast
30	chr8:111325000-111325600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:111325400-111325800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:111325600-111326600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr8:111326600-111334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:111328600-111329000	Enhancers	Fetal Lung	lung
35	chr8:111328800-111329400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:111328800-111329400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:111329400-111332800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:111332800-111333000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:111334000-111334400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:111334000-111334600	Enhancers	HMEC	breast
41	chr8:111334000-111334800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:111334800-111335000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:111335000-111336000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:111336000-111336200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:111336200-111336400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:111339600-111341000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:111340800-111342600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr8:111340800-111342600	Enhancers	Fetal Lung	lung
49	chr8:111341000-111341400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr8:111341000-111341600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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