Variant report

Variant	esv1836974
Chromosome Location	chr6:28376981-28398748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:28392052-28392181	K562	blood:	n/a	n/a
2	ATF1	chr6:28393754-28393889	K562	blood:	n/a	n/a
3	BACH1	chr6:28391979-28392274	K562	blood:	n/a	n/a
4	BATF	chr6:28393720-28394036	GM12878	blood:	n/a	n/a
5	BATF	chr6:28393697-28394153	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:28393774-28394303	GM12878	blood:	n/a	n/a
7	CCNT2	chr6:28393817-28393877	K562	blood:	n/a	n/a
8	CEBPB	chr6:28391902-28392263	K562	blood:	n/a	n/a
9	CEBPB	chr6:28395029-28395299	HepG2	liver:	n/a	chr6:28395187-28395198 chr6:28395141-28395152
10	CEBPB	chr6:28381310-28381575	K562	blood:	n/a	chr6:28381439-28381450
11	CEBPB	chr6:28395067-28395228	Hela-S3	cervix:	n/a	chr6:28395187-28395198 chr6:28395141-28395152
12	CEBPB	chr6:28395080-28395296	IMR90	lung:	n/a	chr6:28395187-28395198 chr6:28395141-28395152
13	CEBPB	chr6:28395081-28395215	K562	blood:	n/a	chr6:28395187-28395198 chr6:28395141-28395152
14	CEBPB	chr6:28381323-28381577	HepG2	liver:	n/a	chr6:28381439-28381450
15	CEBPB	chr6:28395024-28395192	A549	lung:	n/a	chr6:28395141-28395152
16	CEBPB	chr6:28381348-28381604	IMR90	lung:	n/a	chr6:28381439-28381450
17	CEBPD	chr6:28390908-28391427	K562	blood:	n/a	chr6:28391151-28391162
18	EP300	chr6:28392003-28392251	K562	blood:	n/a	n/a
19	FOS	chr6:28391910-28392323	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr6:28391978-28392347	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr6:28391985-28392268	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr6:28391922-28392324	MCF10A-Er-Src	breast:	n/a	n/a
23	FOSL2	chr6:28392018-28392274	MCF-7	breast:	n/a	n/a
24	FOXA2	chr6:28394828-28395017	HepG2	liver:	n/a	n/a
25	GATA1	chr6:28390327-28392412	K562	blood:	n/a	chr6:28391140-28391147 chr6:28391110-28391117 chr6:28391110-28391117 chr6:28391110-28391117 chr6:28391138-28391154 chr6:28391103-28391124 chr6:28391109-28391119
26	GATA3	chr6:28392056-28392256	MCF-7	breast:	n/a	n/a
27	GATA3	chr6:28391882-28392428	SK-N-SH	brain:	n/a	n/a
28	GATA3	chr6:28390860-28391266	MCF-7	breast:	n/a	chr6:28391140-28391147 chr6:28391110-28391117 chr6:28391110-28391117 chr6:28391110-28391117 chr6:28391138-28391154 chr6:28391103-28391124 chr6:28391109-28391119
29	GATA3	chr6:28391874-28392381	MCF-7	breast:	n/a	n/a
30	IKZF1	chr6:28393709-28394170	GM12878	blood:	n/a	n/a
31	IRF1	chr6:28392108-28392126	K562	blood:	n/a	n/a
32	IRF1	chr6:28392049-28392157	K562	blood:	n/a	n/a
33	IRF4	chr6:28393633-28394123	GM12878	blood:	n/a	n/a
34	JUND	chr6:28391946-28392320	K562	blood:	n/a	n/a
35	JUND	chr6:28395886-28395962	HepG2	liver:	n/a	n/a
36	MAFF	chr6:28391956-28392301	K562	blood:	n/a	n/a
37	MAFF	chr6:28393753-28394017	HepG2	liver:	n/a	chr6:28393886-28393904
38	MAFK	chr6:28391938-28392277	K562	blood:	n/a	n/a
39	MAFK	chr6:28393730-28394026	HepG2	liver:	n/a	chr6:28393887-28393902
40	MAFK	chr6:28393777-28394014	HepG2	liver:	n/a	chr6:28393887-28393902
41	MTA3	chr6:28393651-28394168	GM12878	blood:	n/a	n/a
42	MYC	chr6:28390084-28390176	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr6:28392081-28392210	K562	blood:	n/a	n/a
44	NFIC	chr6:28381370-28381748	ECC-1	luminal epithelium:	n/a	n/a
45	NFYB	chr6:28398094-28398298	K562	blood:	n/a	n/a
46	NFYB	chr6:28393952-28393985	GM12878	blood:	n/a	n/a
47	NR2F2	chr6:28398049-28398337	K562	blood:	n/a	chr6:28398229-28398244
48	POLR2A	chr6:28398640-28398720	ProgFib	skin:	n/a	n/a
49	POLR2A	chr6:28397699-28397727	ProgFib	skin:	n/a	n/a
50	POLR2A	chr6:28397894-28398125	ProgFib	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:28356866..28359445-chr6:28388346..28391982,3	K562	blood:
2	chr6:28373595..28375831-chr6:28378815..28380474,2	K562	blood:
3	chr6:28397761..28399629-chr6:28401778..28405817,3	K562	blood:
4	chr6:28392901..28395106-chr6:28398520..28400756,3	K562	blood:
5	chr6:28389572..28392930-chr6:28395042..28397704,3	K562	blood:
6	chr6:28379842..28382776-chr6:28383800..28386316,2	K562	blood:
7	chr6:28349465..28351465-chr6:28394048..28396108,2	MCF-7	breast:
8	chr6:28385891..28388590-chr6:28390011..28392158,2	K562	blood:
9	chr6:28369764..28371489-chr6:28380154..28383821,4	K562	blood:
10	chr6:28370825..28372910-chr6:28390622..28392729,2	MCF-7	breast:
11	chr6:28365314..28368724-chr6:28382074..28385198,3	K562	blood:
12	chr6:28390398..28392930-chr6:28395199..28398373,4	K562	blood:
13	chr6:28385891..28388590-chr6:28390011..28392158,2	K562	blood:
14	chr6:28380471..28382537-chr6:28386259..28388038,2	K562	blood:
15	chr6:28390398..28392930-chr6:28395199..28398373,4	K562	blood:
16	chr6:28376587..28378827-chr6:28380769..28382729,2	K562	blood:
17	chr6:27836090..27837594-chr6:28374724..28377447,2	K562	blood:
18	chr6:28365464..28369045-chr6:28381351..28384382,6	K562	blood:
19	chr6:28389572..28392930-chr6:28395042..28397704,3	K562	blood:
20	chr6:28379842..28382776-chr6:28383800..28386316,2	K562	blood:
21	chr6:28373846..28375488-chr6:28394522..28397398,2	K562	blood:
22	chr6:28392901..28395106-chr6:28398520..28400756,3	K562	blood:
23	chr6:28382729..28384623-chr6:28406130..28408766,2	K562	blood:
24	chr6:28380471..28382537-chr6:28386259..28388038,2	K562	blood:
25	chr6:28356707..28359445-chr6:28388134..28391982,4	K562	blood:
26	chr6:28380846..28382983-chr6:28391973..28394917,2	K562	blood:
27	chr6:28364231..28371937-chr6:28372195..28378158,17	K562	blood:
28	chr6:28380846..28382983-chr6:28391973..28394917,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSCAN23-1	chr6:28392120-28394123	NONHSAT108462
2	lnc-ZSCAN23-1	chr6:28390179-28391617	NONHSAT108462

Variant related genes	Relation type
RNU2-45P	TF binding region
ENSG00000251877	chromatin interactions
ENSG00000158691	chromatin interactions

Extended variants
information (count: 647 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17314865	chr6:28376981-28376982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116820163	chr6:28377009-28377010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553383530	chr6:28377067-28377068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565008759	chr6:28377219-28377220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189895300	chr6:28377290-28377291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140477071	chr6:28377312-28377313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575024025	chr6:28377328-28377329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75881555	chr6:28377389-28377390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529837786	chr6:28377451-28377452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373843896	chr6:28377494-28377495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs546535359	chr6:28377527-28377528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368020101	chr6:28377538-28377539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542311399	chr6:28377612-28377613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566406425	chr6:28377631-28377632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534729884	chr6:28377658-28377659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563896443	chr6:28377678-28377679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575748184	chr6:28377688-28377689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150405966	chr6:28377699-28377700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372190581	chr6:28377829-28377830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183209566	chr6:28377836-28377837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537555449	chr6:28377910-28377911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs557135189	chr6:28377979-28377980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574215488	chr6:28377980-28377981	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs536444828	chr6:28378056-28378057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35218015	chr6:28378093-28378094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546191290	chr6:28378108-28378109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573564599	chr6:28378126-28378127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs72854550	chr6:28378131-28378132	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188853295	chr6:28378179-28378180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575086018	chr6:28378205-28378206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544332450	chr6:28378224-28378225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138185123	chr6:28378251-28378252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529926313	chr6:28378258-28378259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564424344	chr6:28378278-28378279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377310158	chr6:28378297-28378298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528362629	chr6:28378439-28378440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193038415	chr6:28378442-28378443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532295658	chr6:28378452-28378453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552006477	chr6:28378516-28378517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571625898	chr6:28378541-28378542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80340004	chr6:28378542-28378543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75431337	chr6:28378544-28378545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149587951	chr6:28378566-28378567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143311036	chr6:28378616-28378617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553622253	chr6:28378648-28378649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148347206	chr6:28378658-28378659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539346558	chr6:28378668-28378669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201087117	chr6:28378745-28378746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138337717	chr6:28378747-28378748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147389275	chr6:28378749-28378750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28371200-28410400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:28374000-28377200	Enhancers	K562	blood
3	chr6:28376000-28377000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:28377000-28386600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:28377600-28390200	Weak transcription	Fetal Lung	lung
6	chr6:28379400-28389200	Weak transcription	HSMM	muscle
7	chr6:28380800-28390600	Weak transcription	Brain Hippocampus Middle	brain
8	chr6:28381400-28390000	Weak transcription	Fetal Brain Female	brain
9	chr6:28382600-28386600	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:28382800-28387600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:28383400-28390600	Weak transcription	Fetal Stomach	stomach
12	chr6:28383600-28392600	Weak transcription	Brain Germinal Matrix	brain
13	chr6:28383800-28393000	Weak transcription	Fetal Intestine Small	intestine
14	chr6:28384000-28386600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:28384000-28387600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:28384200-28384600	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:28384200-28384600	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr6:28384200-28386800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:28384600-28385200	Active TSS	Placenta	Placenta
20	chr6:28384600-28386800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr6:28384600-28387800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:28384600-28390200	Weak transcription	NH-A	brain
23	chr6:28384600-28410200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr6:28384800-28388000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:28384800-28388400	Weak transcription	Small Intestine	intestine
26	chr6:28384800-28390800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:28385000-28387400	Weak transcription	NHDF-Ad	bronchial
28	chr6:28385000-28390600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:28385200-28390600	Weak transcription	Placenta	Placenta
30	chr6:28385400-28391000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr6:28385400-28391200	Weak transcription	HSMMtube	muscle
32	chr6:28385400-28402000	Weak transcription	Fetal Kidney	kidney
33	chr6:28385400-28402200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr6:28385600-28390800	Weak transcription	Aorta	Aorta
35	chr6:28385600-28390800	Weak transcription	Ovary	ovary
36	chr6:28385600-28410800	Weak transcription	Lung	lung
37	chr6:28385800-28387600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:28385800-28390800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:28385800-28391800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:28386000-28386200	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr6:28386000-28387600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:28386000-28402200	Weak transcription	Osteobl	bone
43	chr6:28386000-28410400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr6:28386200-28390000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:28386200-28390600	Weak transcription	Right Ventricle	heart
46	chr6:28386200-28391000	Weak transcription	Psoas Muscle	Psoas
47	chr6:28386200-28395800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr6:28386600-28387800	Strong transcription	Fetal Muscle Leg	muscle
49	chr6:28386600-28391000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:28386600-28392200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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