Variant report

Variant	nsv967620
Chromosome Location	chr8:100013130-100021334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:100014445-100014796	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:100014442-100014700	K562	blood:	n/a	n/a
3	CEBPB	chr8:100020238-100020477	HepG2	liver:	n/a	chr8:100020326-100020337
4	CEBPB	chr8:100020307-100020524	A549	lung:	n/a	chr8:100020326-100020337
5	CEBPB	chr8:100020307-100020361	K562	blood:	n/a	chr8:100020326-100020337
6	CHD1	chr8:100014776-100014891	GM12878	blood:	n/a	n/a
7	EBF1	chr8:100014604-100014774	GM12878	blood:	n/a	n/a
8	EBF1	chr8:100014492-100014862	GM12878	blood:	n/a	n/a
9	ELF1	chr8:100014368-100014753	GM12878	blood:	n/a	chr8:100014572-100014583
10	EP300	chr8:100014555-100014807	GM12878	blood:	n/a	n/a
11	EP300	chr8:100015624-100015687	GM12878	blood:	n/a	chr8:100015672-100015686
12	ESR1	chr8:100020498-100020728	ECC-1	luminal epithelium:	n/a	n/a
13	ESR1	chr8:100020411-100020757	ECC-1	luminal epithelium:	n/a	n/a
14	IKZF1	chr8:100014616-100014816	GM12878	blood:	n/a	n/a
15	MAFK	chr8:100013105-100013305	HepG2	liver:	n/a	n/a
16	MAFK	chr8:100013115-100013294	HepG2	liver:	n/a	n/a
17	MAZ	chr8:100015568-100015664	GM12878	blood:	n/a	n/a
18	MTA3	chr8:100014417-100015009	GM12878	blood:	n/a	n/a
19	MXI1	chr8:100014504-100014777	GM12878	blood:	n/a	n/a
20	NFATC1	chr8:100014510-100014970	GM12878	blood:	n/a	n/a
21	NFE2	chr8:100014593-100014642	GM12878	blood:	n/a	n/a
22	PBX3	chr8:100015485-100015748	GM12878	blood:	n/a	n/a
23	POLR2A	chr8:100014293-100014309	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr8:100015005-100015280	MCF-7	breast:	n/a	n/a
25	POLR2A	chr8:100015571-100015758	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr8:100016054-100016109	K562	blood:	n/a	n/a
27	POLR2A	chr8:100014591-100015152	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr8:100014437-100015462	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr8:100017448-100017765	K562	blood:	n/a	n/a
30	POLR2A	chr8:100014901-100015101	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr8:100015986-100016027	K562	blood:	n/a	n/a
32	POLR2A	chr8:100015117-100015147	HepG2	liver:	n/a	n/a
33	POLR2A	chr8:100014775-100015178	HCT-116	colon:	n/a	n/a
34	POLR2A	chr8:100020301-100020325	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr8:100017767-100017982	K562	blood:	n/a	n/a
36	POLR2A	chr8:100014753-100015284	K562	blood:	n/a	n/a
37	POLR2A	chr8:100020598-100020745	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr8:100016110-100016212	K562	blood:	n/a	n/a
39	POLR2A	chr8:100016832-100016866	HepG2	liver:	n/a	n/a
40	POLR2A	chr8:100020253-100020262	K562	blood:	n/a	n/a
41	POLR2A	chr8:100020311-100021064	K562	blood:	n/a	n/a
42	POLR2A	chr8:100014694-100014916	ProgFib	skin:	n/a	n/a
43	POLR2A	chr8:100015255-100015317	HepG2	liver:	n/a	n/a
44	POLR2A	chr8:100017698-100017712	K562	blood:	n/a	n/a
45	POLR2A	chr8:100013638-100013816	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr8:100014209-100014347	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr8:100014119-100016931	K562	blood:	n/a	n/a
48	POLR2A	chr8:100014415-100014461	ProgFib	skin:	n/a	n/a
49	POLR2A	chr8:100014953-100014957	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr8:100014968-100015114	Hela-S3	cervix:	n/a	n/a

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:100008104..100010992-chr8:100011648..100013634,2	MCF-7	breast:
2	chr8:100009588..100012990-chr8:100013654..100017766,5	K562	blood:
3	chr8:99956252..99958234-chr8:100019639..100022057,2	MCF-7	breast:
4	chr8:100013073..100014994-chr8:100016917..100018773,2	K562	blood:
5	chr8:100013186..100018258-chr8:100022769..100026424,8	MCF-7	breast:
6	chr8:100011207..100013044-chr8:100013955..100016177,3	K562	blood:
7	chr8:100019090..100021113-chr8:100023467..100025831,2	K562	blood:
8	chr8:100010458..100013760-chr8:100016389..100018197,3	MCF-7	breast:
9	chr8:99989686..99991239-chr8:100020336..100022687,2	MCF-7	breast:
10	chr8:100005341..100007193-chr8:100016588..100018736,2	MCF-7	breast:
11	chr8:100013073..100014994-chr8:100016917..100018773,2	K562	blood:
12	chr8:100020387..100022270-chr8:100223332..100224852,2	MCF-7	breast:
13	chr8:100006551..100008465-chr8:100016441..100018763,2	MCF-7	breast:
14	chr8:99966073..99968633-chr8:100020306..100022554,2	K562	blood:
15	chr8:99952762..99963438-chr8:100019139..100031293,37	MCF-7	breast:
16	chr8:99956762..99958304-chr8:100013613..100016438,2	K562	blood:
17	chr8:99952140..99962153-chr8:100006475..100015090,25	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK3-5	chr8:100018891-100019738	l_3657_chr8:100017408-100021457_testes
2	lnc-STK3-5	chr8:100020741-100021457	l_3657_chr8:100017408-100021457_testes
3	lnc-VPS13B-1	chr8:100008217-100013862	NONHSAT127942
4	lnc-STK3-5	chr8:100017409-100018868	l_3657_chr8:100017408-100021457_testes
5	lnc-VPS13B-1	chr8:100014060-100015451	NONHSAT127942

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000253180	TF binding region
ENSG00000164920	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000263842	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000132549	chromatin interactions

Extended variants
information (count: 286 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10107475	chr8:100013171-100013172	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10955192	chr8:100013209-100013210	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147033387	chr8:100013277-100013278	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs545371544	chr8:100013348-100013349	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs138592207	chr8:100013363-100013364	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs551367862	chr8:100013412-100013413	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs527777188	chr8:100013434-100013435	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs142614157	chr8:100013510-100013511	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs561062068	chr8:100013538-100013539	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs386728141	chr8:100013560-100013561	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs10955193	chr8:100013562-100013563	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs377221242	chr8:100013634-100013635	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs549735849	chr8:100013639-100013640	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs10955194	chr8:100013650-100013651	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs532341073	chr8:100013658-100013659	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs12114454	chr8:100013674-100013675	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565634725	chr8:100013689-100013690	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs534614589	chr8:100013709-100013710	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs548274488	chr8:100013759-100013760	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs568087234	chr8:100013789-100013790	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs536832786	chr8:100013814-100013815	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
22	rs556514925	chr8:100013833-100013834	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs576664611	chr8:100013847-100013848	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs538994900	chr8:100013888-100013889	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs552139045	chr8:100013929-100013930	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs6999016	chr8:100014016-100014017	Weak transcription Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370147018	chr8:100014052-100014053	Weak transcription Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs35383090	chr8:100014062-100014063	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
29	rs371644914	chr8:100014085-100014086	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs572074168	chr8:100014178-100014179	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
31	rs541046957	chr8:100014184-100014185	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs190229059	chr8:100014277-100014278	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs570541150	chr8:100014354-100014355	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs574868000	chr8:100014381-100014382	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs541297192	chr8:100014409-100014410	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs55853273	chr8:100014413-100014414	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs139206366	chr8:100014511-100014512	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs561509279	chr8:100014585-100014586	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs563380953	chr8:100014604-100014605	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs181454690	chr8:100014638-100014639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs552463302	chr8:100014661-100014662	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs559702791	chr8:100014668-100014669	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
43	rs118116465	chr8:100014682-100014683	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
44	rs548237630	chr8:100014719-100014720	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
45	rs568132826	chr8:100014724-100014725	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
46	rs185748404	chr8:100014733-100014734	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
47	rs542759876	chr8:100014744-100014745	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs562530661	chr8:100014773-100014774	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs141695614	chr8:100014818-100014819	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs570104705	chr8:100014901-100014902	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
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
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
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
Multiple myeloma	16461302	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
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
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99987200-100024200	Weak transcription	Osteobl	bone
2	chr8:100003400-100023400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:100006600-100024000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:100007000-100023800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:100007000-100024200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:100007200-100016000	Weak transcription	HSMMtube	muscle
7	chr8:100007200-100023000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:100007200-100023600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:100007200-100024000	Weak transcription	Ovary	ovary
10	chr8:100007200-100024400	Weak transcription	Aorta	Aorta
11	chr8:100007400-100014800	Weak transcription	Adipose Nuclei	Adipose
12	chr8:100007400-100015800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:100007800-100018200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:100008200-100018000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:100008600-100021800	Weak transcription	NHDF-Ad	bronchial
16	chr8:100008600-100024000	Weak transcription	NHLF	lung
17	chr8:100008800-100022400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:100012000-100023000	Weak transcription	Liver	Liver
19	chr8:100012000-100023200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:100012200-100023800	Weak transcription	HSMM	muscle
21	chr8:100012400-100013800	Weak transcription	Pancreas	Pancrea
22	chr8:100012400-100023400	Weak transcription	Fetal Lung	lung
23	chr8:100012800-100014200	Weak transcription	Fetal Heart	heart
24	chr8:100013600-100017200	Weak transcription	Stomach Smooth Muscle	stomach
25	chr8:100013800-100014200	Enhancers	Pancreas	Pancrea
26	chr8:100014000-100014200	Active TSS	Primary B cells from cord blood	blood
27	chr8:100014200-100014400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:100014200-100014400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:100014200-100014400	Weak transcription	Pancreas	Pancrea
30	chr8:100014200-100014400	Enhancers	Small Intestine	intestine
31	chr8:100014200-100014400	Enhancers	GM12878-XiMat	blood
32	chr8:100014200-100015200	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr8:100014200-100015200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr8:100014200-100015400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr8:100014200-100015400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr8:100014200-100015400	Enhancers	Fetal Heart	heart
37	chr8:100014200-100015600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr8:100014200-100016000	Enhancers	Primary hematopoietic stem cells	blood
39	chr8:100014200-100016200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:100014200-100017400	Weak transcription	Fetal Muscle Leg	muscle
41	chr8:100014200-100023000	Weak transcription	Primary B cells from cord blood	blood
42	chr8:100014400-100014800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:100014400-100015000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr8:100014400-100015000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr8:100014400-100015000	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr8:100014400-100015200	Enhancers	Primary T cells from cord blood	blood
47	chr8:100014400-100015200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr8:100014400-100015200	Enhancers	Pancreas	Pancrea
49	chr8:100014400-100015200	Flanking Active TSS	GM12878-XiMat	blood
50	chr8:100014400-100015400	Enhancers	Thymus	Thymus

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