Variant report

Variant	esv2829863
Chromosome Location	chr6:74976178-75040446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:74999604-75000012	IMR90	lung:	n/a	chr6:74999810-74999827
2	CEBPZ	chr6:74985570-74985693	HepG2	liver:	n/a	n/a
3	CTCF	chr6:74990120-74990270	HRPEpiC	eye:	n/a	n/a
4	CTCF	chr6:74990163-74990258	Medullo	brain:	n/a	n/a
5	CTCF	chr6:74990060-74990210	HCFaa	heart:	n/a	n/a
6	CTCF	chr6:74990080-74990230	GM12872	blood:	n/a	n/a
7	CTCF	chr6:74989800-74989950	HEK293	kidney:	n/a	n/a
8	CTCF	chr6:74990100-74990250	BJ	skin:	n/a	n/a
9	CTCF	chr6:74990100-74990250	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr6:75020056-75020103	LNCaP	prostate:	n/a	n/a
11	CTCF	chr6:74990060-74990210	HMF	breast:	n/a	n/a
12	CTCF	chr6:74989520-74989670	AG10803	skin:	n/a	chr6:74989638-74989647
13	CTCF	chr6:74990068-74990326	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:75019605-75019681	GM10248	blood:	n/a	n/a
15	CTCF	chr6:74990120-74990309	K562	blood:	n/a	n/a
16	CTCF	chr6:74989540-74989690	AG04450	lung:	n/a	chr6:74989638-74989647
17	CTCF	chr6:74989680-74989830	HAc	cerebellar:	n/a	n/a
18	CTCF	chr6:74990120-74990270	K562	blood:	n/a	n/a
19	CTCF	chr6:74999180-74999330	NHLF	lung:	n/a	chr6:74999245-74999258
20	CTCF	chr6:74999830-74999898	IMR90	lung:	n/a	n/a
21	CTCF	chr6:74990161-74990212	GM10266	blood:	n/a	n/a
22	CTCF	chr6:74989520-74989670	NHEK	skin:	n/a	chr6:74989638-74989647
23	CTCF	chr6:74990135-74990271	Fibrobl	skin:	n/a	n/a
24	CTCF	chr6:74989540-74989690	Caco-2	colon:	n/a	chr6:74989638-74989647
25	CTCF	chr6:74989648-74989684	ProgFib	skin:	n/a	n/a
26	CTCF	chr6:74990040-74990190	GM12868	blood:	n/a	n/a
27	CTCF	chr6:74990200-74990350	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr6:74990110-74990292	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:74990140-74990290	AG09309	skin:	n/a	n/a
30	CTCF	chr6:74989560-74989710	HA-sp	spinal cord:	n/a	chr6:74989638-74989647
31	CTCF	chr6:75019980-75020130	GM12873	blood:	n/a	n/a
32	CTCF	chr6:74990180-74990330	HVMF	connective:	n/a	n/a
33	CTCF	chr6:74989540-74989690	GM12873	blood:	n/a	chr6:74989638-74989647
34	CTCF	chr6:74989500-74989650	AG10803	skin:	n/a	chr6:74989638-74989647
35	CTCF	chr6:75019920-75020070	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr6:74989840-74989990	RPTEC	kidney:	n/a	n/a
37	CTCF	chr6:74990140-74990290	RPTEC	kidney:	n/a	n/a
38	CTCF	chr6:74990120-74990270	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:74990140-74990290	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr6:74990120-74990270	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr6:74989380-74989530	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr6:74990080-74990230	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr6:74990120-74990270	AG09319	gingival:	n/a	n/a
44	CTCF	chr6:74990140-74990290	HCT-116	colon:	n/a	n/a
45	CTCF	chr6:74990100-74990250	HFF	foreskin:	n/a	n/a
46	CTCF	chr6:75020000-75020150	HCT-116	colon:	n/a	n/a
47	CTCF	chr6:74990040-74990190	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:74989580-74989730	GM12872	blood:	n/a	chr6:74989638-74989647
49	CTCF	chr6:74990160-74990310	GM06990	blood:	n/a	n/a
50	CTCF	chr6:75019980-75020130	HEK293	kidney:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74978996-74979046	HRCEpiC	kidney:	n/a
2	chr6:74978996-74979046	HRCEpiC	kidney:	n/a
3	chr6:74998385-74998435	Hela-S3	cervix:	n/a
4	chr6:74978996-74979046	GM12878	blood:	n/a
5	chr6:74987753-74987803	AG09309	skin:	n/a
6	chr6:74998385-74998435	PrEC	prostate:	n/a
7	chr6:74978996-74979046	SK-N-SH_RA	brain:	n/a
8	chr6:74987753-74987803	HNPCEpiC	eye:	n/a
9	chr6:74998385-74998435	HAEpiC	amniotic membrane:	n/a
10	chr6:74987753-74987803	HCT-116	colon:	n/a
11	chr6:74978996-74979046	IMR90	lung:	fetal
12	chr6:74978996-74979046	LNCaP	prostate:	n/a
13	chr6:74998385-74998435	BJ	skin:	n/a
14	chr6:74998385-74998435	NHDF-neo	bronchial:	n/a
15	chr6:74998385-74998435	HEEpiC	esophagus:	n/a
16	chr6:74987753-74987803	HCM	heart:	n/a
17	chr6:74998385-74998435	LNCaP	prostate:	n/a
18	chr6:74987753-74987803	ProgFib	skin:	n/a
19	chr6:74987753-74987803	HMEC	breast:	n/a
20	chr6:74998385-74998435	Caco-2	colon:	n/a
21	chr6:74998385-74998435	AG04450	lung:	fetal
22	chr6:74987753-74987803	GM12878	blood:	n/a
23	chr6:74978996-74979046	SAEC	small airway:	n/a
24	chr6:74998385-74998435	Jurkat	blood:	n/a
25	chr6:74987753-74987803	HRE	kidney:	n/a
26	chr6:74998385-74998435	HRPEpiC	eye:	n/a
27	chr6:74987753-74987803	GM12891	blood:	n/a
28	chr6:74998385-74998435	HUVEC	blood vessel:	n/a
29	chr6:74987753-74987803	AG04450	lung:	fetal
30	chr6:74978996-74979046	AG09319	gingival:	n/a
31	chr6:74978996-74979046	GM06990	blood:	n/a
32	chr6:74998385-74998435	MCF-7	breast:	n/a
33	chr6:74987753-74987803	PFSK-1	brain:	n/a
34	chr6:74978996-74979046	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:74987753-74987803	H1-hESC	embryonic stem cell:	embryo
36	chr6:74998385-74998435	HRE	kidney:	n/a
37	chr6:74978996-74979046	MCF10A-Er-Src	breast:	n/a
38	chr6:74998385-74998435	K562	blood:	n/a
39	chr6:74998385-74998435	HCPEpiC	choroid plexus:	n/a
40	chr6:74987753-74987803	NB4	blood:	n/a
41	chr6:74998385-74998435	AG09309	skin:	n/a
42	chr6:74978996-74979046	NHDF-neo	bronchial:	n/a
43	chr6:74998385-74998435	SK-N-MC	brain:	n/a
44	chr6:74998385-74998435	ProgFib	skin:	n/a
45	chr6:74978996-74979046	SK-N-SH	brain:	n/a
46	chr6:74987753-74987803	GM19239	blood:	n/a
47	chr6:74998385-74998435	MCF10A-Er-Src	breast:	n/a
48	chr6:74987753-74987803	SK-N-SH_RA	brain:	n/a
49	chr6:74987753-74987803	K562	blood:	n/a
50	chr6:74987753-74987803	HCPEpiC	choroid plexus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:
2	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:
3	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
4	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:
5	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
6	chr19:18479342..18480148-chr6:75021400..75022173,2	MCF-7	breast:
7	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000217178	TF binding region
ENSG00000217178	CpG island

Extended variants
information (count: 1246 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1246 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1387417	chr6:74976600-74976601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs72953713	chr6:74976611-74976612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532749800	chr6:74976638-74976639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181126250	chr6:74976647-74976648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569619867	chr6:74976750-74976751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77617485	chr6:74976831-74976832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548712199	chr6:74976834-74976835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538389711	chr6:74976841-74976842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184411329	chr6:74976864-74976865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534513703	chr6:74976865-74976866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552809911	chr6:74976903-74976904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373015233	chr6:74976905-74976906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571535426	chr6:74976956-74976957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1387418	chr6:74976958-74976959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189344824	chr6:74976960-74976961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575096481	chr6:74976969-74976970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181971249	chr6:74976970-74976971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78317015	chr6:74976993-74976994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539310367	chr6:74976995-74976996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377325170	chr6:74977060-74977061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371805214	chr6:74977064-74977065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572731392	chr6:74977100-74977101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9352084	chr6:74977142-74977143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10805997	chr6:74977170-74977171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs144773154	chr6:74977176-74977177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12524014	chr6:74977180-74977181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs148568227	chr6:74977211-74977212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141198947	chr6:74977251-74977252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186192870	chr6:74977254-74977255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9352085	chr6:74977282-74977283	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548624207	chr6:74977287-74977288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560661021	chr6:74977290-74977291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528237757	chr6:74977291-74977292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561396485	chr6:74977292-74977293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546795714	chr6:74977320-74977321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529101340	chr6:74977327-74977328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547536023	chr6:74977344-74977345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571381723	chr6:74977376-74977377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375379132	chr6:74977385-74977386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550641440	chr6:74977428-74977429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79101102	chr6:74977432-74977433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537445499	chr6:74977487-74977488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76453076	chr6:74977496-74977497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369644918	chr6:74977521-74977522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574195441	chr6:74977538-74977539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535200335	chr6:74977573-74977574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114651519	chr6:74977574-74977575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555283531	chr6:74977576-74977577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545683514	chr6:74977583-74977584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1387419	chr6:74977604-74977605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	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
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74976600-74976800	Enhancers	Fetal Muscle Leg	muscle
2	chr6:74976800-74979000	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:74978200-74979400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:74979000-74979400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:74979000-74979400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:74979000-74979400	Enhancers	Fetal Muscle Leg	muscle
7	chr6:74979000-74979400	Enhancers	NHDF-Ad	bronchial
8	chr6:74979000-74979600	Enhancers	Fetal Stomach	stomach
9	chr6:74979200-74979400	Bivalent Enhancer	HSMMtube	muscle
10	chr6:74979400-74979600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:74979400-74987400	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:74979600-74983800	Weak transcription	Fetal Stomach	stomach
13	chr6:74981200-74981600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr6:74983800-74984200	Enhancers	Fetal Stomach	stomach
15	chr6:74987200-74987800	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:74987200-74988000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:74987200-74988000	Enhancers	Rectal Smooth Muscle	rectum
18	chr6:74987200-74988000	Enhancers	HSMMtube	muscle
19	chr6:74987200-74988400	Enhancers	Fetal Kidney	kidney
20	chr6:74987200-74988800	Enhancers	Placenta Amnion	Placenta Amnion
21	chr6:74987400-74987600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:74987400-74987600	Enhancers	NHDF-Ad	bronchial
23	chr6:74987400-74987800	Enhancers	Brain Hippocampus Middle	brain
24	chr6:74987400-74987800	Enhancers	Colon Smooth Muscle	Colon
25	chr6:74987400-74987800	Enhancers	Fetal Heart	heart
26	chr6:74987400-74988000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:74987400-74988000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr6:74987400-74988000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr6:74987400-74988000	Enhancers	Brain Germinal Matrix	brain
30	chr6:74987400-74988000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr6:74987400-74988000	Enhancers	Fetal Lung	lung
32	chr6:74987400-74988000	Enhancers	Fetal Muscle Leg	muscle
33	chr6:74987400-74988000	Enhancers	Psoas Muscle	Psoas
34	chr6:74987400-74988000	Enhancers	Right Ventricle	heart
35	chr6:74987400-74988400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:74987400-74988600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr6:74987600-74989600	Weak transcription	NHDF-Ad	bronchial
38	chr6:74988000-74992600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:74989600-74990000	Enhancers	NHDF-Ad	bronchial
40	chr6:74992000-74992200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:74992000-74992200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:74992600-74994800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:74993000-74993600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:74993200-74994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:74993400-74994200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr6:74993800-74994400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:74994800-74996000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr6:74995600-74996400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:74996000-74996600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:74996000-74997200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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