Variant report

Variant	esv3411569
Chromosome Location	chr6:68997654-69198750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:69039700-69039839	K562	blood:	n/a	n/a
2	ARID3A	chr6:69178389-69178711	K562	blood:	n/a	n/a
3	ATF1	chr6:69178169-69178665	K562	blood:	n/a	n/a
4	BACH1	chr6:69196503-69196515	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr6:69178467-69178669	K562	blood:	n/a	n/a
6	CEBPB	chr6:69178485-69178781	MCF-7	breast:	n/a	n/a
7	CEBPB	chr6:69189397-69189527	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:69178503-69178771	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:69178223-69178778	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:69083900-69083906	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:69178501-69178787	K562	blood:	n/a	n/a
12	CEBPB	chr6:69151992-69152254	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:69107953-69108153	K562	blood:	n/a	n/a
14	CEBPD	chr6:69178296-69178761	K562	blood:	n/a	n/a
15	CEBPD	chr6:69178276-69178811	K562	blood:	n/a	n/a
16	CHD2	chr6:69071181-69071483	K562	blood:	n/a	n/a
17	CTCF	chr6:69053841-69054184	T-47D	breast:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
18	CTCF	chr6:69023940-69024090	GM12873	blood:	n/a	n/a
19	CTCF	chr6:69178560-69178710	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr6:69178420-69178690	A549	lung:	n/a	n/a
21	CTCF	chr6:69053900-69054050	GM06990	blood:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
22	CTCF	chr6:69178540-69178690	GM12875	blood:	n/a	n/a
23	CTCF	chr6:69023972-69024058	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr6:69178520-69178628	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr6:69153720-69153870	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr6:69178580-69178730	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr6:69023900-69024050	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr6:69178544-69178704	GM13977	blood:	n/a	n/a
29	CTCF	chr6:69023783-69024203	K562	blood:	n/a	n/a
30	CTCF	chr6:69053900-69054050	HPF	lung:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
31	CTCF	chr6:69023920-69024070	GM12871	blood:	n/a	n/a
32	CTCF	chr6:69178498-69178723	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:69053962-69054039	Spleen_OC	spleen:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
34	CTCF	chr6:69110440-69110590	GM12872	blood:	n/a	n/a
35	CTCF	chr6:69110417-69110561	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:69178528-69178679	HepG2	liver:	n/a	n/a
37	CTCF	chr6:69153700-69153850	GM12864	blood:	n/a	n/a
38	CTCF	chr6:69053920-69054070	GM12874	blood:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
39	CTCF	chr6:69110389-69110605	Gliobla	brain:	n/a	n/a
40	CTCF	chr6:69023960-69024110	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr6:69110386-69110586	GM19238	blood:	n/a	n/a
42	CTCF	chr6:69178419-69178789	K562	blood:	n/a	chr6:69178734-69178742
43	CTCF	chr6:69053920-69054070	GM12871	blood:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
44	CTCF	chr6:69153680-69153830	NHEK	skin:	n/a	n/a
45	CTCF	chr6:69053842-69054132	MCF-7	breast:	n/a	chr6:69053991-69054007 chr6:69053993-69054002 chr6:69053992-69054013 chr6:69053990-69054008 chr6:69053993-69054006
46	CTCF	chr6:69023880-69024030	AG10803	skin:	n/a	n/a
47	CTCF	chr6:69110397-69110601	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:69153660-69153810	Caco-2	colon:	n/a	n/a
49	CTCF	chr6:69153740-69153890	HCT-116	colon:	n/a	n/a
50	CTCF	chr6:69110380-69110530	HRE	kidney:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:69174891..69177006-chr6:69177848..69180556,2	K562	blood:
2	chr6:69188166..69190733-chr6:69192752..69194576,2	K562	blood:
3	chr6:69040879..69043282-chr6:69043307..69044925,2	K562	blood:
4	chr3:73158464..73161460-chr6:69141039..69142539,2	K562	blood:
5	chr6:69182580..69184340-chr6:69184575..69186290,2	K562	blood:
6	chr6:69131492..69134265-chr6:69138928..69141362,2	MCF-7	breast:
7	chr6:69053724..69054431-chr6:69178564..69179099,2	K562	blood:
8	chr17:41400752..41402306-chr6:69141039..69142539,2	MCF-7	breast:
9	chr6:69182580..69184340-chr6:69184575..69186290,2	K562	blood:
10	chr6:68597928..68599571-chr6:69004230..69006877,2	K562	blood:
11	chr6:69025794..69029820-chr6:69036149..69040025,3	K562	blood:
12	chr6:69053885..69054455-chr6:69178429..69178979,2	MCF-7	breast:
13	chr4:157762860..157763615-chr6:69116691..69117521,2	K562	blood:
14	chr6:68947374..68949377-chr6:69045424..69047013,2	MCF-7	breast:
15	chr6:69187451..69191074-chr6:69191437..69194576,4	K562	blood:
16	chr6:69018177..69020747-chr6:69022471..69025294,3	K562	blood:
17	chr6:69053724..69054431-chr6:69178564..69179099,2	K562	blood:
18	chr6:69053946..69055088-chr6:69178263..69178883,3	MCF-7	breast:
19	chr6:69018177..69020747-chr6:69022471..69025294,3	K562	blood:
20	chr22:20918726..20919648-chr6:69136151..69136812,2	MCF-7	breast:
21	chr6:69187451..69191074-chr6:69191437..69194576,4	K562	blood:
22	chr6:69053703..69054300-chr6:69207678..69208508,2	MCF-7	breast:
23	chr6:67774843..67776777-chr6:69022561..69024613,2	MCF-7	breast:
24	chr6:69053685..69054306-chr6:69488036..69488952,2	MCF-7	breast:
25	chr6:69148448..69150705-chr6:69177431..69180205,2	K562	blood:
26	chr6:69046456..69047956-chr6:69051262..69053757,2	K562	blood:
27	chr6:69053885..69054455-chr6:69178429..69178979,2	MCF-7	breast:
28	chr6:68599013..68600726-chr6:69023481..69026040,2	K562	blood:
29	chr6:69148448..69150705-chr6:69177431..69180205,2	K562	blood:
30	chr6:69040879..69043282-chr6:69043307..69044925,2	K562	blood:
31	chr6:69053595..69054445-chr6:69282510..69283038,2	K562	blood:
32	chr6:69073717..69075281-chr6:69077349..69080314,2	K562	blood:
33	chr6:69073717..69075281-chr6:69077349..69080314,2	K562	blood:
34	chr6:69131492..69134265-chr6:69138928..69141362,2	MCF-7	breast:
35	chr6:68591982..68594330-chr6:69016783..69018367,2	K562	blood:
36	chr6:69191363..69194136-chr6:69196139..69198220,2	K562	blood:
37	chr6:69188166..69190733-chr6:69192752..69194576,2	K562	blood:
38	chr6:69191363..69194136-chr6:69196139..69198220,2	K562	blood:
39	chr6:68597012..68600726-chr6:69022767..69026249,4	K562	blood:
40	chr6:69174891..69177006-chr6:69177848..69180556,2	K562	blood:
41	chr6:69053946..69055088-chr6:69178263..69178883,3	MCF-7	breast:
42	chr6:69046456..69047956-chr6:69051262..69053757,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL713998.1-6	chr6:69096404-69096512	NONHSAT113403
2	lnc-AL713998.1-6	chr6:69093558-69093685	NONHSAT113403
3	lnc-AL713998.1-1	chr6:69039683-69039791	XLOC_005757
4	lnc-AL713998.1-6	chr6:69033113-69033228	NONHSAT113403
5	lnc-AL713998.1-1	chr6:69036837-69036964	XLOC_005757

No data

Variant related genes	Relation type
ENSG00000266675	TF binding region
ENSG00000226497	TF binding region
ENSG00000227706	chromatin interactions
ENSG00000226497	chromatin interactions
ENSG00000223247	chromatin interactions
DKK1	miRNA target sites
DIXDC1	miRNA target sites

Extended variants
information (count: 1929 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369493698	chr6:69004264-69004265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs142530994	chr6:69004266-69004267	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370235075	chr6:69004295-69004296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555605066	chr6:69004321-69004322	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35744075	chr6:69004327-69004328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79241989	chr6:69004338-69004339	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200915964	chr6:69004353-69004354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144242921	chr6:69004376-69004377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs67792403	chr6:69004385-69004386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199576617	chr6:69004386-69004387	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192336936	chr6:69004392-69004393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150952091	chr6:69004436-69004437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560648397	chr6:69004473-69004474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558362074	chr6:69004492-69004493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs578261955	chr6:69004500-69004501	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184471783	chr6:69004511-69004512	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs554397228	chr6:69004524-69004525	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12201325	chr6:69004525-69004526	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79714604	chr6:69004528-69004529	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140795813	chr6:69004587-69004588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189762548	chr6:69004588-69004589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181151597	chr6:69004667-69004668	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9363883	chr6:69004671-69004672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185985766	chr6:69004682-69004683	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552582781	chr6:69004701-69004702	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527441625	chr6:69004710-69004711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11752995	chr6:69004774-69004775	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs567014276	chr6:69004778-69004779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189013785	chr6:69004802-69004803	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181410741	chr6:69004804-69004805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187209190	chr6:69004856-69004857	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538342320	chr6:69004866-69004867	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558432799	chr6:69004873-69004874	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113293136	chr6:69004886-69004887	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571748810	chr6:69004907-69004908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534372208	chr6:69004944-69004945	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150131541	chr6:69004977-69004978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376968572	chr6:69004992-69004993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79438127	chr6:69005015-69005016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574257434	chr6:69005033-69005034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146732780	chr6:69005053-69005054	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192096412	chr6:69005065-69005066	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555736056	chr6:69005070-69005071	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575771716	chr6:69005086-69005087	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544712434	chr6:69005107-69005108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564591823	chr6:69005109-69005110	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13191626	chr6:69005127-69005128	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564368657	chr6:69005141-69005142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541186685	chr6:69005210-69005211	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs71555385	chr6:69005222-69005223	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69011600-69014000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:69020800-69021200	Active TSS	K562	blood
3	chr6:69028600-69029200	Enhancers	K562	blood
4	chr6:69068400-69068600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:69071000-69072400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:69073400-69073800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:69073800-69074000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:69074000-69074600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:69074000-69074600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr6:69074000-69074800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:69074000-69074800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:69079200-69079600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:69081600-69084200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:69084200-69084800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:69084800-69085000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:69085800-69086200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:69094600-69094800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr6:69094800-69095400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr6:69118200-69118800	Enhancers	Fetal Brain Male	brain
20	chr6:69118800-69119200	Weak transcription	Fetal Brain Male	brain
21	chr6:69119200-69120000	Enhancers	Fetal Brain Male	brain
22	chr6:69120000-69120600	Weak transcription	Fetal Brain Male	brain
23	chr6:69120600-69120800	Enhancers	Fetal Brain Male	brain
24	chr6:69126200-69126400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:69137600-69138400	Enhancers	NH-A	brain
26	chr6:69139800-69142400	Weak transcription	Stomach Mucosa	stomach
27	chr6:69147600-69148000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:69154800-69155000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:69155200-69155800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:69155800-69156000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:69156000-69156600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:69156800-69157000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:69157000-69157400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr6:69161800-69167400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:69165600-69166200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:69175400-69175800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:69175400-69176000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:69181800-69182400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:69181800-69182400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:69182000-69182200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr6:69182400-69183400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:69182400-69183400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr6:69182400-69185600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:69183400-69183800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr6:69183400-69184200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:69184200-69185800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:69185600-69187400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:69185800-69186400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:69185800-69186800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:69185800-69187600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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