Variant report

Variant	nsv891290
Chromosome Location	chr8:111280576-111377089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

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	CEBPB	chr8:111348693-111348897	A549	lung:	n/a	n/a
4	CEBPB	chr8:111326108-111326428	A549	lung:	n/a	chr8:111326272-111326283
5	CEBPB	chr8:111311633-111311681	A549	lung:	n/a	chr8:111311652-111311663
6	CEBPB	chr8:111326135-111326438	IMR90	lung:	n/a	chr8:111326272-111326283
7	CEBPB	chr8:111311551-111311683	H1-hESC	embryonic stem cell:	n/a	chr8:111311652-111311663
8	CEBPB	chr8:111311571-111311766	HepG2	liver:	n/a	chr8:111311652-111311663
9	CEBPB	chr8:111326111-111326430	HepG2	liver:	n/a	chr8:111326272-111326283
10	CEBPB	chr8:111326176-111326371	K562	blood:	n/a	chr8:111326272-111326283
11	CEBPB	chr8:111346863-111346939	HepG2	liver:	n/a	n/a
12	CTCF	chr8:111367120-111367270	BE2_C	brain:	n/a	n/a
13	CTCF	chr8:111367080-111367230	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr8:111303274-111303371	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:111367804-111367837	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:111367040-111367190	HMEC	breast:	n/a	n/a
17	CTCF	chr8:111311154-111311208	Lung_OC	lung:	n/a	n/a
18	CTCF	chr8:111367140-111367290	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr8:111367020-111367170	RPTEC	kidney:	n/a	n/a
20	CTCF	chr8:111345480-111345630	GM06990	blood:	n/a	n/a
21	CTCF	chr8:111365500-111365650	HBMEC	blood vessel:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
22	CTCF	chr8:111365580-111365730	HCT-116	colon:	n/a	n/a
23	CTCF	chr8:111365540-111365690	HMEC	breast:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
24	CTCF	chr8:111365485-111365682	LNCaP	prostate:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
25	CTCF	chr8:111365520-111365670	BE2_C	brain:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
26	CTCF	chr8:111367151-111367225	Gliobla	brain:	n/a	n/a
27	CTCF	chr8:111365553-111365662	Spleen_OC	spleen:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
28	CTCF	chr8:111365310-111365799	MCF-7	breast:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
29	CTCF	chr8:111365421-111365737	GM12878	blood:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
30	CTCF	chr8:111365480-111365630	HPAF	blood vessel:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
31	CTCF	chr8:111367844-111367845	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:111367140-111367290	A549	lung:	n/a	n/a
33	CTCF	chr8:111365500-111365650	HEEpiC	esophagus:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
34	CTCF	chr8:111365514-111365656	LNCaP	prostate:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
35	CTCF	chr8:111367100-111367250	Caco-2	colon:	n/a	n/a
36	CTCF	chr8:111365525-111365664	Pancreas_OC	pancreas:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
37	CTCF	chr8:111365960-111366110	BE2_C	brain:	n/a	n/a
38	CTCF	chr8:111366940-111367383	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:111299840-111299990	HPF	lung:	n/a	n/a
40	CTCF	chr8:111365451-111365739	H1-hESC	embryonic stem cell:	n/a	chr8:111365573-111365591 chr8:111365575-111365596
41	CTCF	chr8:111367160-111367310	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:111365880-111366030	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:111365660-111365810	HMEC	breast:	n/a	n/a
44	CTCF	chr8:111367102-111367253	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:111367120-111367270	HMEC	breast:	n/a	n/a
46	CTCF	chr8:111367100-111367250	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr8:111367100-111367250	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr8:111367153-111367260	ProgFib	skin:	n/a	n/a
49	CTCF	chr8:111365420-111365570	HMEC	breast:	n/a	n/a
50	CTCF	chr8:111365560-111365710	HEEpiC	esophagus:	n/a	chr8:111365573-111365591 chr8:111365575-111365596

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111342449-111342499	HRCEpiC	kidney:	n/a
2	chr8:111342449-111342499	SKMC	muscle:	n/a
3	chr8:111342449-111342499	HAEpiC	amniotic membrane:	n/a
4	chr8:111342449-111342499	ProgFib	skin:	n/a
5	chr8:111342449-111342499	SAEC	small airway:	n/a
6	chr8:111342449-111342499	AG10803	skin:	n/a
7	chr8:111342449-111342499	CMK	blood:	n/a
8	chr8:111342449-111342499	SK-N-SH	brain:	n/a
9	chr8:111342449-111342499	HEK293	kidney:	embryo
10	chr8:111342449-111342499	NT2-D1	testis:	n/a
11	chr8:111342449-111342499	AG09319	gingival:	n/a
12	chr8:111342449-111342499	AG09309	skin:	n/a
13	chr8:111342449-111342499	HEEpiC	esophagus:	n/a
14	chr8:111342449-111342499	MCF10A-Er-Src	breast:	n/a
15	chr8:111342449-111342499	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:111342449-111342499	NHDF-neo	bronchial:	n/a
17	chr8:111342449-111342499	GM12892	blood:	n/a
18	chr8:111342449-111342499	ECC-1	luminal epithelium:	n/a
19	chr8:111342449-111342499	HepG2	liver:	n/a
20	chr8:111342449-111342499	NHBE	bronchial:	n/a
21	chr8:111342449-111342499	HCM	heart:	n/a
22	chr8:111342449-111342499	HIPEpiC	eye:	n/a
23	chr8:111342449-111342499	SK-N-SH_RA	brain:	n/a
24	chr8:111342449-111342499	IMR90	lung:	fetal
25	chr8:111342449-111342499	HCF	heart:	n/a
26	chr8:111342449-111342499	MCF-7	breast:	n/a
27	chr8:111342449-111342499	Hela-S3	cervix:	n/a
28	chr8:111342449-111342499	HNPCEpiC	eye:	n/a
29	chr8:111342449-111342499	H1-hESC	embryonic stem cell:	embryo
30	chr8:111342449-111342499	NB4	blood:	n/a
31	chr8:111342449-111342499	K562	blood:	n/a
32	chr8:111342449-111342499	BJ	skin:	n/a
33	chr8:111342449-111342499	ovcar-3	ovarian:	n/a
34	chr8:111342449-111342499	GM19239	blood:	n/a
35	chr8:111342449-111342499	AG04449	skin:	fetal
36	chr8:111342449-111342499	HUVEC	blood vessel:	n/a
37	chr8:111342449-111342499	AG04450	lung:	fetal
38	chr8:111342449-111342499	HRE	kidney:	n/a
39	chr8:111342449-111342499	SK-N-MC	brain:	n/a
40	chr8:111342449-111342499	Caco-2	colon:	n/a
41	chr8:111342449-111342499	AoSMC	blood vessel:	n/a
42	chr8:111342449-111342499	LNCaP	prostate:	n/a
43	chr8:111342449-111342499	RPTEC	kidney:	n/a
44	chr8:111342449-111342499	HCPEpiC	choroid plexus:	n/a
45	chr8:111342449-111342499	Jurkat	blood:	n/a
46	chr8:111342449-111342499	Hepatocyte	liver:	n/a
47	chr8:111342449-111342499	A549	lung:	n/a
48	chr8:111342449-111342499	GM12891	blood:	n/a
49	chr8:111342449-111342499	NH-A	brain:	n/a
50	chr8:111342449-111342499	PFSK-1	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
2	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
3	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
4	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
5	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
6	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
7	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
8	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
9	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
10	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
11	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
12	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
13	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:
14	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:
15	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
16	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
17	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:
18	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 2425 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2425 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545928818	chr8:111299610-111299611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562455012	chr8:111299637-111299638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531175810	chr8:111299683-111299684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547806846	chr8:111299725-111299726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368434232	chr8:111299761-111299762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543850819	chr8:111299775-111299776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538603221	chr8:111299893-111299894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563677720	chr8:111299894-111299895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547667661	chr8:111299928-111299929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577300122	chr8:111299930-111299931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62528074	chr8:111299964-111299965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs398047380	chr8:111299965-111299966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578106063	chr8:111299974-111299975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545356491	chr8:111299976-111299977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374304867	chr8:111299993-111299994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138462330	chr8:111301264-111301265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535697286	chr8:111301265-111301266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555049515	chr8:111301353-111301354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571669208	chr8:111301389-111301390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540683679	chr8:111301456-111301457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143272530	chr8:111301519-111301520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183238455	chr8:111301559-111301560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564282809	chr8:111301627-111301628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543980040	chr8:111301671-111301672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12682400	chr8:111301718-111301719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12056621	chr8:111301719-111301720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114453148	chr8:111301741-111301742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34410454	chr8:111301744-111301745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374926036	chr8:111301767-111301768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12682422	chr8:111301774-111301775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549451528	chr8:111301781-111301782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549626405	chr8:111302433-111302434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569631640	chr8:111302449-111302450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377484339	chr8:111302461-111302462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546617265	chr8:111302471-111302472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs16880581	chr8:111302478-111302479	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566551482	chr8:111302497-111302498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531126326	chr8:111302504-111302505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557731355	chr8:111302520-111302521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373569396	chr8:111302595-111302596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77574672	chr8:111302616-111302617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564360567	chr8:111302623-111302624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537051448	chr8:111302637-111302638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117695015	chr8:111302659-111302660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146253364	chr8:111302698-111302699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193140166	chr8:111302736-111302737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559737064	chr8:111302737-111302738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546296242	chr8:111302739-111302740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77628031	chr8:111302744-111302745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78211653	chr8:111302753-111302754	Enhancers	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:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111299600-111300000	Enhancers	Fetal Intestine Large	intestine
2	chr8:111301200-111301600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:111301200-111301800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr8:111301400-111301800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:111302400-111304800	Enhancers	Fetal Brain Male	brain
6	chr8:111303200-111306200	Enhancers	Fetal Brain Female	brain
7	chr8:111303800-111304000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:111304400-111305400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr8:111304800-111305200	Weak transcription	Fetal Brain Male	brain
10	chr8:111305200-111306000	Enhancers	Fetal Brain Male	brain
11	chr8:111305400-111305800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr8:111310800-111311000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:111311000-111322400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:111321800-111324000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:111322200-111324200	Enhancers	HMEC	breast
16	chr8:111322400-111323000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:111322400-111324200	Enhancers	NHEK	skin
18	chr8:111322600-111324000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:111323000-111323400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:111323400-111325000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:111324200-111334000	Weak transcription	HMEC	breast
22	chr8:111325000-111325600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:111325400-111325800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:111325600-111326600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:111326600-111334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:111328600-111329000	Enhancers	Fetal Lung	lung
27	chr8:111328800-111329400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:111328800-111329400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:111329400-111332800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:111332800-111333000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:111334000-111334400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:111334000-111334600	Enhancers	HMEC	breast
33	chr8:111334000-111334800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:111334800-111335000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:111335000-111336000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:111336000-111336200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:111336200-111336400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:111339600-111341000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:111340800-111342600	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr8:111340800-111342600	Enhancers	Fetal Lung	lung
41	chr8:111341000-111341400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr8:111341000-111341600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:111341000-111342400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:111341000-111342400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:111341200-111342400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:111341400-111341800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr8:111341400-111342200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr8:111341400-111342200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:111341400-111342400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr8:111341600-111342200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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