Variant report

Variant	esv1813061
Chromosome Location	chr6:26877074-26947622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1344)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26924747-26924778	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:26925619-26925955	HepG2	liver:	n/a	n/a
3	ATF1	chr6:26923925-26924305	K562	blood:	n/a	n/a
4	ATF2	chr6:26923841-26924229	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:26923847-26924306	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:26923942-26924231	GM12878	blood:	n/a	n/a
7	BACH1	chr6:26924664-26924943	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:26920524-26920940	GM12878	blood:	n/a	n/a
9	BATF	chr6:26925319-26925723	GM12878	blood:	n/a	n/a
10	BATF	chr6:26879415-26880231	GM12878	blood:	n/a	n/a
11	BATF	chr6:26940264-26940496	GM12878	blood:	n/a	chr6:26940350-26940360
12	BATF	chr6:26924423-26924966	GM12878	blood:	n/a	n/a
13	BATF	chr6:26877375-26877691	GM12878	blood:	n/a	n/a
14	BATF	chr6:26881525-26881784	GM12878	blood:	n/a	n/a
15	BATF	chr6:26880945-26881148	GM12878	blood:	n/a	n/a
16	BATF	chr6:26923787-26924103	GM12878	blood:	n/a	n/a
17	BATF	chr6:26923753-26924403	GM12878	blood:	n/a	n/a
18	BATF	chr6:26919159-26919394	GM12878	blood:	n/a	n/a
19	BATF	chr6:26919077-26919488	GM12878	blood:	n/a	n/a
20	BATF	chr6:26921657-26921936	GM12878	blood:	n/a	n/a
21	BATF	chr6:26896004-26896253	GM12878	blood:	n/a	n/a
22	BATF	chr6:26896440-26896670	GM12878	blood:	n/a	chr6:26896493-26896502
23	BATF	chr6:26917064-26917394	GM12878	blood:	n/a	n/a
24	BATF	chr6:26911356-26911600	GM12878	blood:	n/a	n/a
25	BATF	chr6:26879420-26880201	GM12878	blood:	n/a	n/a
26	BATF	chr6:26918546-26918790	GM12878	blood:	n/a	n/a
27	BATF	chr6:26911148-26911328	GM12878	blood:	n/a	n/a
28	BATF	chr6:26928990-26929230	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
29	BATF	chr6:26929003-26929176	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
30	BATF	chr6:26925030-26925340	GM12878	blood:	n/a	n/a
31	BATF	chr6:26922534-26922741	GM12878	blood:	n/a	n/a
32	BATF	chr6:26923128-26923365	GM12878	blood:	n/a	n/a
33	BATF	chr6:26889952-26890170	GM12878	blood:	n/a	n/a
34	BATF	chr6:26878925-26879156	GM12878	blood:	n/a	n/a
35	BATF	chr6:26923172-26923556	GM12878	blood:	n/a	n/a
36	BATF	chr6:26917548-26917891	GM12878	blood:	n/a	n/a
37	BCL11A	chr6:26923759-26924025	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:26922379-26922777	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:26879919-26880155	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:26919192-26919425	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:26923669-26925780	GM12878	blood:	n/a	n/a
42	BCL11A	chr6:26888476-26888667	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:26921673-26921928	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:26925060-26925245	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:26890806-26891033	GM12878	blood:	n/a	n/a
46	BCL11A	chr6:26917021-26917371	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:26917073-26917429	GM12878	blood:	n/a	n/a
48	BCL11A	chr6:26879581-26880185	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:26928959-26929218	GM12878	blood:	n/a	chr6:26929119-26929128 chr6:26929120-26929129
50	BCL11A	chr6:26917588-26917845	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26923983-26924033	GM12878	blood:	n/a
2	chr6:26924767-26924817	HCF	heart:	n/a
3	chr6:26924550-26924600	HPAEpiC	pulmonary alveolar:	n/a
4	chr6:26924767-26924817	SK-N-SH	brain:	n/a
5	chr6:26924550-26924600	HEEpiC	esophagus:	n/a
6	chr6:26924767-26924817	LNCaP	prostate:	n/a
7	chr6:26924767-26924817	PrEC	prostate:	n/a
8	chr6:26923983-26924033	A549	lung:	n/a
9	chr6:26924550-26924600	HRPEpiC	eye:	n/a
10	chr6:26914441-26914491	NH-A	brain:	n/a
11	chr6:26923983-26924033	SKMC	muscle:	n/a
12	chr6:26924767-26924817	HIPEpiC	eye:	n/a
13	chr6:26923983-26924033	NHDF-neo	bronchial:	n/a
14	chr6:26923983-26924033	HEK293	kidney:	embryo
15	chr6:26914441-26914491	SAEC	small airway:	n/a
16	chr6:26924767-26924817	ECC-1	luminal epithelium:	n/a
17	chr6:26924550-26924600	HepG2	liver:	n/a
18	chr6:26923983-26924033	NT2-D1	testis:	n/a
19	chr6:26924550-26924600	MCF10A-Er-Src	breast:	n/a
20	chr6:26924550-26924600	HRCEpiC	kidney:	n/a
21	chr6:26914441-26914491	AG04450	lung:	fetal
22	chr6:26923983-26924033	HL-60	blood:	n/a
23	chr6:26924767-26924817	GM12878	blood:	n/a
24	chr6:26923983-26924033	HIPEpiC	eye:	n/a
25	chr6:26923983-26924033	IMR90	lung:	fetal
26	chr6:26924767-26924817	IMR90	lung:	fetal
27	chr6:26923983-26924033	GM12892	blood:	n/a
28	chr6:26914441-26914491	T-47D	breast:	n/a
29	chr6:26924550-26924600	IMR90	lung:	fetal
30	chr6:26914441-26914491	NT2-D1	testis:	n/a
31	chr6:26924550-26924600	HMEC	breast:	n/a
32	chr6:26914441-26914491	Hela-S3	cervix:	n/a
33	chr6:26924767-26924817	Hepatocyte	liver:	n/a
34	chr6:26914441-26914491	Jurkat	blood:	n/a
35	chr6:26914441-26914491	HEEpiC	esophagus:	n/a
36	chr6:26924767-26924817	U87	brain:	n/a
37	chr6:26924767-26924817	HepG2	liver:	n/a
38	chr6:26924550-26924600	Jurkat	blood:	n/a
39	chr6:26923983-26924033	U87	brain:	n/a
40	chr6:26923983-26924033	AoSMC	blood vessel:	n/a
41	chr6:26914441-26914491	ovcar-3	ovarian:	n/a
42	chr6:26923983-26924033	ovcar-3	ovarian:	n/a
43	chr6:26914441-26914491	HepG2	liver:	n/a
44	chr6:26924550-26924600	GM12878	blood:	n/a
45	chr6:26924767-26924817	HRCEpiC	kidney:	n/a
46	chr6:26923983-26924033	HepG2	liver:	n/a
47	chr6:26924550-26924600	GM06990	blood:	n/a
48	chr6:26924550-26924600	LNCaP	prostate:	n/a
49	chr6:26914441-26914491	GM12892	blood:	n/a
50	chr6:26923983-26924033	BJ	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26922078..26923970-chr6:27032946..27034480,2	K562	blood:
2	chr6:26923847..26925381-chr6:26927830..26930168,2	MCF-7	breast:
3	chr6:26156738..26158730-chr6:26923909..26926382,2	K562	blood:
4	chr6:26878821..26880986-chr6:26986600..26988197,2	MCF-7	breast:
5	chr6:26923074..26925467-chr6:26986570..26988926,2	K562	blood:
6	chr6:26922448..26924229-chr6:27062597..27064654,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AG-3	chr6:26936797-26942146	ENSG00000224843.2
2	lnc-HIST1H2AG-3	chr6:26924772-26924962	ENSG00000224843.2
3	lnc-HIST1H2AG-3	chr6:26936797-26936850	XLOC_005216
4	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108320
5	lnc-HIST1H2AG-3	chr6:26936237-26936301	NONHSAT108320
6	lnc-HIST1H2AG-3	chr6:26924771-26924962	ENSG00000224843.2
7	lnc-HIST1H2AG-3	chr6:26924879-26924962	XLOC_005216
8	lnc-HIST1H2AG-3	chr6:26936237-26936301	XLOC_005216
9	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2
10	lnc-HIST1H2BJ-10	chr6:26924168-26924285	NONHSAT108318
11	lnc-HIST1H2AG-3	chr6:26926892-26926895	NONHSAT108319
12	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108319
13	lnc-HIST1H2AG-3	chr6:26936241-26936301	NONHSAT108319
14	lnc-HIST1H2BJ-10	chr6:26892898-26893054	NONHSAT108318
15	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2

No data

Variant related genes	Relation type
LINC00240	TF binding region
GUSBP2	TF binding region
LINC00240	CpG island
GUSBP2	CpG island
ENSG00000158373	chromatin interactions
ENSG00000238621	chromatin interactions
ENSG00000224843	chromatin interactions
ENSG00000241549	chromatin interactions

Extended variants
information (count: 788 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:788 , 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	rs146708102	chr6:26878832-26878833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561906884	chr6:26878856-26878857	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10946865	chr6:26878864-26878865	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs541245154	chr6:26878889-26878890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12216370	chr6:26878930-26878931	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs140262324	chr6:26878946-26878947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549793916	chr6:26879033-26879034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545339533	chr6:26879112-26879113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143992976	chr6:26879200-26879201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184079029	chr6:26879293-26879294	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200854615	chr6:26879304-26879305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188618823	chr6:26879392-26879393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146411508	chr6:26879395-26879396	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201638305	chr6:26879419-26879420	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370620466	chr6:26879431-26879432	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140622591	chr6:26879452-26879453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs56853796	chr6:26879467-26879468	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540217963	chr6:26879558-26879559	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs537186234	chr6:26879591-26879592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191613371	chr6:26879606-26879607	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183074089	chr6:26879609-26879610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12189753	chr6:26879620-26879621	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs138319473	chr6:26879662-26879663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572310480	chr6:26879693-26879694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540831385	chr6:26879763-26879764	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370332692	chr6:26879771-26879772	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149202178	chr6:26879809-26879810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543572525	chr6:26879821-26879822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563256937	chr6:26879838-26879839	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113046593	chr6:26879883-26879884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187087578	chr6:26879887-26879888	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542629709	chr6:26879904-26879905	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559749133	chr6:26879935-26879936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528789196	chr6:26879968-26879969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544325568	chr6:26879978-26879979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551670445	chr6:26880022-26880023	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571553853	chr6:26880032-26880033	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530888907	chr6:26880100-26880101	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562502396	chr6:26880146-26880147	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs3999347	chr6:26880157-26880158	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs9467928	chr6:26880192-26880193	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560371121	chr6:26880211-26880212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs553343627	chr6:26880220-26880221	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563819840	chr6:26880261-26880262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191828498	chr6:26880358-26880359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557963471	chr6:26880360-26880361	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527618470	chr6:26880385-26880386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143067312	chr6:26880386-26880387	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs6925804	chr6:26880413-26880414	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs557063271	chr6:26880445-26880446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26888200-26893800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:26889400-26893600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:26889600-26891600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:26889600-26891800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:26889800-26894400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:26890200-26892800	Weak transcription	Adipose Nuclei	Adipose
7	chr6:26890200-26894400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:26890400-26893200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:26890600-26892800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:26890600-26893000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:26890600-26893000	Weak transcription	Fetal Kidney	kidney
12	chr6:26891600-26891800	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:26891800-26892200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:26891800-26893800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:26892200-26893800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:26911600-26912600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:26914200-26914800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:26922000-26923000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:26922800-26923000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:26922800-26923000	Enhancers	K562	blood
21	chr6:26923000-26923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:26923000-26924000	Weak transcription	K562	blood
23	chr6:26923400-26925400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr6:26923800-26924000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:26923800-26924400	Active TSS	GM12878-XiMat	blood
26	chr6:26923800-26925000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:26923800-26925000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:26923800-26925000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:26923800-26925000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:26923800-26925000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:26923800-26925000	Active TSS	Left Ventricle	heart
32	chr6:26923800-26925000	Active TSS	HUVEC	blood vessel
33	chr6:26923800-26925200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:26923800-26925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:26923800-26925200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:26923800-26925400	Active TSS	H1 Cell Line	embryonic stem cell
37	chr6:26923800-26925400	Active TSS	H9 Cell Line	embryonic stem cell
38	chr6:26923800-26925400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:26923800-26925400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:26923800-26925400	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr6:26923800-26925400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:26923800-26925400	Active TSS	Brain Anterior Caudate	brain
43	chr6:26923800-26925400	Active TSS	Brain Cingulate Gyrus	brain
44	chr6:26923800-26925400	Active TSS	Right Ventricle	heart
45	chr6:26923800-26925400	Active TSS	Stomach Smooth Muscle	stomach
46	chr6:26923800-26925400	Active TSS	NHDF-Ad	bronchial
47	chr6:26923800-26925600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:26923800-26925600	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr6:26923800-26925600	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr6:26923800-26925600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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