Variant report

Variant	nsv464023
Chromosome Location	chr6:114071720-114114057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:114107472-114107672	HepG2	liver:	n/a	n/a
2	ATF2	chr6:114098079-114098698	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:114084252-114085561	GM12878	blood:	n/a	n/a
4	ATF2	chr6:114076591-114077689	GM12878	blood:	n/a	n/a
5	ATF2	chr6:114076677-114077634	GM12878	blood:	n/a	n/a
6	ATF2	chr6:114084877-114085515	GM12878	blood:	n/a	n/a
7	ATF2	chr6:114097931-114098688	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:114084474-114084793	GM12878	blood:	n/a	n/a
9	BATF	chr6:114076683-114077423	GM12878	blood:	n/a	n/a
10	BATF	chr6:114074610-114074905	GM12878	blood:	n/a	n/a
11	BATF	chr6:114084963-114085567	GM12878	blood:	n/a	n/a
12	BATF	chr6:114085007-114085388	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:114098158-114098581	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr6:114085057-114085378	GM12878	blood:	n/a	chr6:114085176-114085185
15	BCL11A	chr6:114098145-114098576	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr6:114076736-114077424	GM12878	blood:	n/a	chr6:114076871-114076880
17	BCL3	chr6:114085055-114085506	GM12878	blood:	n/a	chr6:114085176-114085185
18	BCL3	chr6:114076678-114077464	GM12878	blood:	n/a	chr6:114076871-114076880
19	BCLAF1	chr6:114076632-114077540	GM12878	blood:	n/a	chr6:114076871-114076880
20	BCLAF1	chr6:114084935-114085509	GM12878	blood:	n/a	chr6:114085176-114085185
21	BHLHE40	chr6:114078237-114078534	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:114076944-114077559	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:114075781-114075831	GM12878	blood:	n/a	n/a
24	CEBPB	chr6:114095684-114095993	A549	lung:	n/a	n/a
25	CEBPB	chr6:114084875-114085617	HCT-116	colon:	n/a	n/a
26	CEBPB	chr6:114085065-114085451	A549	lung:	n/a	n/a
27	CEBPB	chr6:114076723-114077646	GM12878	blood:	n/a	chr6:114077252-114077263
28	CEBPB	chr6:114075720-114075994	A549	lung:	n/a	n/a
29	CEBPB	chr6:114079366-114079562	HepG2	liver:	n/a	chr6:114079505-114079516
30	CEBPB	chr6:114085038-114085427	A549	lung:	n/a	n/a
31	CEBPB	chr6:114095504-114096041	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:114077108-114077365	HepG2	liver:	n/a	chr6:114077252-114077263
33	CEBPB	chr6:114084848-114085649	GM12878	blood:	n/a	n/a
34	CEBPB	chr6:114075833-114075988	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:114084458-114085466	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:114079452-114079557	H1-hESC	embryonic stem cell:	n/a	chr6:114079505-114079516
37	CEBPB	chr6:114095643-114096010	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:114085047-114085429	IMR90	lung:	n/a	n/a
39	CEBPB	chr6:114095477-114096147	HCT-116	colon:	n/a	n/a
40	CEBPB	chr6:114098171-114098523	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr6:114080035-114080184	GM12878	blood:	n/a	n/a
42	CHD2	chr6:114076949-114077448	GM12878	blood:	n/a	n/a
43	CHD2	chr6:114085115-114085397	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr6:114098075-114098664	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:114098126-114098654	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr6:114097993-114098680	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr6:114098204-114098653	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr6:114078341-114078444	GM10266	blood:	n/a	n/a
49	CTCF	chr6:114089377-114089404	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr6:114106835-114106904	GM13976	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114098428-114098478	SKMC	muscle:	n/a
2	chr6:114098428-114098478	K562	blood:	n/a
3	chr6:114098428-114098478	CMK	blood:	n/a
4	chr6:114098428-114098478	ovcar-3	ovarian:	n/a
5	chr6:114098428-114098478	LNCaP	prostate:	n/a
6	chr6:114098428-114098478	SK-N-SH_RA	brain:	n/a
7	chr6:114098428-114098478	HUVEC	blood vessel:	n/a
8	chr6:114098428-114098478	ProgFib	skin:	n/a
9	chr6:114098428-114098478	Hela-S3	cervix:	n/a
10	chr6:114098428-114098478	HCM	heart:	n/a
11	chr6:114098428-114098478	MCF10A-Er-Src	breast:	n/a
12	chr6:114098428-114098478	AoSMC	blood vessel:	n/a
13	chr6:114098428-114098478	Jurkat	blood:	n/a
14	chr6:114098428-114098478	PANC-1	pancreas:	n/a
15	chr6:114098428-114098478	AG09319	gingival:	n/a
16	chr6:114098428-114098478	GM12878	blood:	n/a
17	chr6:114098428-114098478	AG04449	skin:	fetal
18	chr6:114098428-114098478	U87	brain:	n/a
19	chr6:114098428-114098478	HCF	heart:	n/a
20	chr6:114098428-114098478	AG04450	lung:	fetal
21	chr6:114098428-114098478	H1-hESC	embryonic stem cell:	embryo
22	chr6:114098428-114098478	T-47D	breast:	n/a
23	chr6:114098428-114098478	HRE	kidney:	n/a
24	chr6:114098428-114098478	SK-N-SH	brain:	n/a
25	chr6:114098428-114098478	NH-A	brain:	n/a
26	chr6:114098428-114098478	SAEC	small airway:	n/a
27	chr6:114098428-114098478	BE2_C	brain:	n/a
28	chr6:114098428-114098478	HRCEpiC	kidney:	n/a
29	chr6:114098428-114098478	NB4	blood:	n/a
30	chr6:114098428-114098478	AG09309	skin:	n/a
31	chr6:114098428-114098478	HMEC	breast:	n/a
32	chr6:114098428-114098478	HNPCEpiC	eye:	n/a
33	chr6:114098428-114098478	PrEC	prostate:	n/a
34	chr6:114098428-114098478	SK-N-MC	brain:	n/a
35	chr6:114098428-114098478	Caco-2	colon:	n/a
36	chr6:114098428-114098478	AG10803	skin:	n/a
37	chr6:114098428-114098478	NHDF-neo	bronchial:	n/a
38	chr6:114098428-114098478	IMR90	lung:	fetal
39	chr6:114098428-114098478	HepG2	liver:	n/a
40	chr6:114098428-114098478	GM12892	blood:	n/a
41	chr6:114098428-114098478	HCPEpiC	choroid plexus:	n/a
42	chr6:114098428-114098478	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:114098428-114098478	GM19239	blood:	n/a
44	chr6:114098428-114098478	NHBE	bronchial:	n/a
45	chr6:114098428-114098478	Hepatocyte	liver:	n/a
46	chr6:114098428-114098478	HRPEpiC	eye:	n/a
47	chr6:114098428-114098478	GM06990	blood:	n/a
48	chr6:114098428-114098478	A549	lung:	n/a
49	chr6:114098428-114098478	ECC-1	luminal epithelium:	n/a
50	chr6:114098428-114098478	HEK293	kidney:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:114017203..114020038-chr6:114083854..114086336,2	MCF-7	breast:
2	chr6:114080493..114083851-chr6:114178361..114180752,3	MCF-7	breast:
3	chr6:114079000..114080556-chr6:114084506..114086465,2	K562	blood:
4	chr6:114091896..114093988-chr6:114177482..114179843,2	MCF-7	breast:
5	chr6:114078677..114080335-chr6:114081487..114084433,2	MCF-7	breast:
6	chr6:114078677..114080335-chr6:114081487..114084433,2	MCF-7	breast:
7	chr6:114084994..114086741-chr6:114178527..114180154,2	MCF-7	breast:
8	chr6:114079000..114080556-chr6:114084506..114086465,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-2	chr6:114113032-114113346	ENSG00000231912
2	lnc-HDAC2-8	chr6:114077910-114077969	NONHSAT114568
3	lnc-HDAC2-6	chr6:114113032-114113346	ENSG00000231912.2

No data

Variant related genes	Relation type
ENSG00000253091	TF binding region
ENSG00000253091	CpG island
ENSG00000155130	chromatin interactions

Extended variants
information (count: 1552 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7765004	chr6:114071720-114071721	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78812202	chr6:114071762-114071763	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs570675657	chr6:114071771-114071772	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs112124660	chr6:114071910-114071911	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs12204831	chr6:114071954-114071955	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187125450	chr6:114071977-114071978	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs191465064	chr6:114072122-114072123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557630063	chr6:114072135-114072136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139172020	chr6:114072162-114072163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6930835	chr6:114072164-114072165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145238123	chr6:114072250-114072251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372039562	chr6:114072255-114072256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560810967	chr6:114072267-114072268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62416038	chr6:114072295-114072296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113301101	chr6:114072328-114072329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540302686	chr6:114072337-114072338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374706311	chr6:114072358-114072359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386408308	chr6:114072359-114072360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386408309	chr6:114072374-114072375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397887220	chr6:114072375-114072376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183607560	chr6:114072386-114072387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113879048	chr6:114072398-114072399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190470310	chr6:114072403-114072404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529392513	chr6:114072457-114072458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550648985	chr6:114072481-114072482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs36000791	chr6:114072482-114072483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs193218261	chr6:114072491-114072492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34037801	chr6:114072502-114072503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185491079	chr6:114072512-114072513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541477328	chr6:114072538-114072539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368017109	chr6:114072539-114072540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570691079	chr6:114072544-114072545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534899384	chr6:114072657-114072658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77451665	chr6:114072702-114072703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568056050	chr6:114072738-114072739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146096627	chr6:114072755-114072756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557935816	chr6:114072758-114072759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557095907	chr6:114072913-114072914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548054669	chr6:114072918-114072919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577778301	chr6:114072937-114072938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558314972	chr6:114072941-114072942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573485404	chr6:114072949-114072950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549431138	chr6:114072952-114072953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540917085	chr6:114072953-114072954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145723021	chr6:114072984-114072985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12111107	chr6:114073023-114073024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148924432	chr6:114073038-114073039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62416039	chr6:114073039-114073040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58004831	chr6:114073048-114073049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs71566202	chr6:114073077-114073078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114067000-114075800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:114067400-114079200	Weak transcription	Placenta	Placenta
3	chr6:114070800-114072400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:114070800-114072600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:114071000-114072000	Enhancers	Primary hematopoietic stem cells	blood
6	chr6:114071000-114072000	Enhancers	HepG2	liver
7	chr6:114071000-114072200	Enhancers	Primary B cells from peripheral blood	blood
8	chr6:114071200-114071800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr6:114071200-114072000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr6:114071600-114072000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:114071800-114079200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr6:114072000-114072200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr6:114072000-114077000	Weak transcription	HepG2	liver
14	chr6:114072000-114079600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:114072200-114075000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:114072600-114074800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:114074000-114076800	Enhancers	GM12878-XiMat	blood
18	chr6:114074800-114075000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:114075000-114075400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:114075000-114077600	Enhancers	Primary B cells from peripheral blood	blood
21	chr6:114075400-114078600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:114075600-114077400	Enhancers	Primary B cells from cord blood	blood
23	chr6:114075800-114077600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr6:114076200-114077000	Enhancers	Fetal Muscle Trunk	muscle
25	chr6:114076600-114077600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:114076800-114077000	Enhancers	Psoas Muscle	Psoas
27	chr6:114076800-114077200	Enhancers	Brain Angular Gyrus	brain
28	chr6:114076800-114077200	Enhancers	Brain Hippocampus Middle	brain
29	chr6:114076800-114077400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:114076800-114077400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr6:114076800-114077400	Enhancers	NHDF-Ad	bronchial
32	chr6:114076800-114077600	Enhancers	Fetal Muscle Leg	muscle
33	chr6:114076800-114077600	Flanking Active TSS	GM12878-XiMat	blood
34	chr6:114076800-114077800	Enhancers	Duodenum Mucosa	Duodenum
35	chr6:114077000-114077400	Enhancers	Brain Anterior Caudate	brain
36	chr6:114077000-114077400	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr6:114077000-114077400	Enhancers	Brain Substantia Nigra	brain
38	chr6:114077000-114077400	Enhancers	HepG2	liver
39	chr6:114077000-114077600	Enhancers	HSMM	muscle
40	chr6:114077000-114077800	Enhancers	HSMMtube	muscle
41	chr6:114077000-114085000	Weak transcription	Psoas Muscle	Psoas
42	chr6:114077400-114079600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr6:114077400-114080400	Weak transcription	Primary B cells from cord blood	blood
44	chr6:114077600-114080200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr6:114077600-114080200	Weak transcription	Fetal Muscle Leg	muscle
46	chr6:114077600-114080800	Enhancers	GM12878-XiMat	blood
47	chr6:114077600-114083800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:114077600-114084600	Weak transcription	HSMM	muscle
49	chr6:114078600-114079600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:114079200-114080600	Enhancers	Placenta	Placenta

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