Variant report

Variant	nsv526617
Chromosome Location	chr6:29571545-29576393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:1404)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:29572620-29572770	HepG2	liver:	n/a	n/a
2	MXI1	chr6:29571560-29572284	SK-N-SH	brain:	n/a	n/a
3	POLR2A	chr6:29574534-29574715	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr6:29576305-29576315	K562	blood:	n/a	n/a
5	POLR2A	chr6:29574069-29574155	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr6:29574531-29574630	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr6:29571891-29572346	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr6:29575184-29575395	K562	blood:	n/a	n/a
9	POLR2A	chr6:29573412-29573556	K562	blood:	n/a	n/a
10	POLR2A	chr6:29573584-29575173	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr6:29572647-29573116	K562	blood:	n/a	n/a
12	POLR2A	chr6:29571885-29572504	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr6:29573368-29573500	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr6:29571808-29571959	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr6:29572209-29572391	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr6:29571927-29572144	K562	blood:	n/a	n/a
17	POLR2A	chr6:29573681-29574020	K562	blood:	n/a	n/a
18	POLR2A	chr6:29572652-29572895	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr6:29572585-29572823	K562	blood:	n/a	n/a
20	POLR2A	chr6:29572211-29572377	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr6:29575050-29575201	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr6:29575561-29575972	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr6:29573232-29573645	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr6:29576011-29576760	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr6:29574650-29574665	H1-hESC	embryonic stem cell:	n/a	n/a
26	REST	chr6:29571784-29572026	SK-N-SH	brain:	n/a	n/a
27	ZNF263	chr6:29572433-29572704	HEK293-T-REx	kidney:	n/a	chr6:29572526-29572547 chr6:29572576-29572585 chr6:29572476-29572497 chr6:29572525-29572534

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29574225-29574275	GM12891	blood:	n/a
2	chr6:29574225-29574275	GM12891	blood:	n/a
3	chr6:29572379-29572429	HL-60	blood:	n/a
4	chr6:29573253-29573303	HL-60	blood:	n/a
5	chr6:29574918-29574968	IMR90	lung:	fetal
6	chr6:29572379-29572429	HCF	heart:	n/a
7	chr6:29573253-29573303	PANC-1	pancreas:	n/a
8	chr6:29572333-29572383	MCF-7	breast:	n/a
9	chr6:29572333-29572383	NHBE	bronchial:	n/a
10	chr6:29574953-29575003	AG09309	skin:	n/a
11	chr6:29572219-29572269	AG09309	skin:	n/a
12	chr6:29574918-29574968	HCT-116	colon:	n/a
13	chr6:29573014-29573064	HNPCEpiC	eye:	n/a
14	chr6:29571875-29571925	A549	lung:	n/a
15	chr6:29576329-29576379	HAEpiC	amniotic membrane:	n/a
16	chr6:29574225-29574275	NB4	blood:	n/a
17	chr6:29573377-29573427	PFSK-1	brain:	n/a
18	chr6:29574810-29574860	MCF10A-Er-Src	breast:	n/a
19	chr6:29572219-29572269	AG04450	lung:	fetal
20	chr6:29573377-29573427	MCF-7	breast:	n/a
21	chr6:29572346-29572396	NT2-D1	testis:	n/a
22	chr6:29575128-29575178	AG04449	skin:	fetal
23	chr6:29574715-29574765	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:29573014-29573064	HCPEpiC	choroid plexus:	n/a
25	chr6:29576329-29576379	SK-N-SH	brain:	n/a
26	chr6:29572373-29572423	SK-N-SH	brain:	n/a
27	chr6:29574225-29574275	MCF-7	breast:	n/a
28	chr6:29572373-29572423	PFSK-1	brain:	n/a
29	chr6:29573029-29573079	HL-60	blood:	n/a
30	chr6:29574700-29574750	LNCaP	prostate:	n/a
31	chr6:29573089-29573139	SK-N-MC	brain:	n/a
32	chr6:29573089-29573139	HAEpiC	amniotic membrane:	n/a
33	chr6:29574953-29575003	HEEpiC	esophagus:	n/a
34	chr6:29574953-29575003	MCF10A-Er-Src	breast:	n/a
35	chr6:29574810-29574860	Hepatocyte	liver:	n/a
36	chr6:29572379-29572429	HRCEpiC	kidney:	n/a
37	chr6:29573377-29573427	GM12892	blood:	n/a
38	chr6:29574810-29574860	HRE	kidney:	n/a
39	chr6:29572346-29572396	RPTEC	kidney:	n/a
40	chr6:29572333-29572383	HUVEC	blood vessel:	n/a
41	chr6:29574715-29574765	SK-N-SH	brain:	n/a
42	chr6:29575145-29575195	ovcar-3	ovarian:	n/a
43	chr6:29573377-29573427	SK-N-SH_RA	brain:	n/a
44	chr6:29574918-29574968	BE2_C	brain:	n/a
45	chr6:29576329-29576379	SKMC	muscle:	n/a
46	chr6:29573377-29573427	AG04450	lung:	fetal
47	chr6:29574225-29574275	HUVEC	blood vessel:	n/a
48	chr6:29574810-29574860	HAEpiC	amniotic membrane:	n/a
49	chr6:29575566-29575616	HNPCEpiC	eye:	n/a
50	chr6:29572346-29572396	A549	lung:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29564159..29568485-chr6:29574849..29577852,4	K562	blood:
2	chr6:29564780..29575712-chr6:29592511..29597522,14	K562	blood:
3	chr6:29572757..29580903-chr6:29593317..29599166,10	K562	blood:
4	chr6:29571256..29575251-chr6:29575309..29583536,9	K562	blood:
5	chr6:29567658..29569553-chr6:29570192..29572225,2	K562	blood:
6	chr6:29574743..29577585-chr6:29585500..29587353,2	K562	blood:
7	chr6:29571256..29575251-chr6:29575309..29583536,9	K562	blood:
8	chr6:29564159..29568485-chr6:29574849..29577852,3	K562	blood:
9	chr6:29566358..29568865-chr6:29570413..29572313,3	K562	blood:
10	chr6:29566782..29572750-chr6:29592808..29598864,8	K562	blood:

No data

Variant related genes	Relation type
GABBR1	TF binding region
GABBR1	CpG island
ENSG00000204681	chromatin interactions

Extended variants
information (count: 162 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:162 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2076483	chr6:29571545-29571546	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs55941866	chr6:29571577-29571578	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575184595	chr6:29571585-29571586	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10946999	chr6:29571609-29571610	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs554120922	chr6:29571617-29571618	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574135751	chr6:29571701-29571702	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540320147	chr6:29571704-29571705	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559996464	chr6:29571707-29571708	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs3025639	chr6:29571741-29571742	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182062647	chr6:29571745-29571746	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565552223	chr6:29571770-29571771	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531212010	chr6:29571843-29571844	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115268184	chr6:29571883-29571884	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567652171	chr6:29571998-29571999	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs56106029	chr6:29572064-29572065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547023786	chr6:29572085-29572086	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566859268	chr6:29572131-29572132	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538792076	chr6:29572132-29572133	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12525400	chr6:29572160-29572161	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs577843081	chr6:29572177-29572178	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs56062033	chr6:29572183-29572184	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs200818597	chr6:29572193-29572194	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201638805	chr6:29572210-29572211	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537732808	chr6:29572261-29572262	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369069690	chr6:29572262-29572263	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140401546	chr6:29572279-29572280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560254994	chr6:29572332-29572333	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145419499	chr6:29572373-29572374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs202144350	chr6:29572377-29572378	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539857403	chr6:29572409-29572410	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374757081	chr6:29572419-29572420	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543633411	chr6:29572434-29572435	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112562687	chr6:29572465-29572466	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553796810	chr6:29572481-29572482	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190005485	chr6:29572487-29572488	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545914368	chr6:29572490-29572491	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565465963	chr6:29572507-29572508	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377713883	chr6:29572525-29572526	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531172373	chr6:29572549-29572550	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181702336	chr6:29572561-29572562	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561568814	chr6:29572573-29572574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369743030	chr6:29572643-29572644	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530061014	chr6:29572646-29572647	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138053745	chr6:29572684-29572685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12189690	chr6:29572706-29572707	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200753831	chr6:29572789-29572790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376501403	chr6:29572802-29572803	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370705474	chr6:29572806-29572807	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373263590	chr6:29572816-29572817	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532476879	chr6:29572822-29572823	Strong transcription Weak transcription Genic enhancers	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
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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29561600-29571600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:29561800-29571600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:29561800-29573200	Weak transcription	HSMMtube	muscle
4	chr6:29562000-29571800	Weak transcription	Left Ventricle	heart
5	chr6:29562000-29572600	Weak transcription	Fetal Heart	heart
6	chr6:29565600-29572200	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr6:29566400-29595200	Weak transcription	Right Atrium	heart
8	chr6:29566600-29587000	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr6:29566800-29571800	Strong transcription	Fetal Brain Female	brain
10	chr6:29566800-29572000	Weak transcription	Pancreas	Pancrea
11	chr6:29566800-29572400	Weak transcription	HUVEC	blood vessel
12	chr6:29566800-29584600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:29566800-29590000	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr6:29566800-29590600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:29567000-29571800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:29567000-29589800	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr6:29567200-29571800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:29567200-29571800	Weak transcription	Esophagus	oesophagus
19	chr6:29567200-29589400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr6:29567200-29589800	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:29567400-29572000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr6:29567600-29574600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:29567600-29583800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:29567600-29592400	Strong transcription	Fetal Stomach	stomach
25	chr6:29567600-29595400	Weak transcription	A549	lung
26	chr6:29567800-29571600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:29567800-29572000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:29567800-29582800	Strong transcription	Ovary	ovary
29	chr6:29567800-29584600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:29568000-29571600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:29568000-29572200	Weak transcription	Primary T cells from cord blood	blood
32	chr6:29568000-29574600	Weak transcription	HSMM	muscle
33	chr6:29568200-29572000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr6:29568200-29572800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:29568400-29572400	Weak transcription	Dnd41	blood
36	chr6:29568400-29582600	Strong transcription	HMEC	breast
37	chr6:29568400-29583600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:29568600-29595200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:29568800-29572200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:29568800-29578000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:29568800-29583200	Strong transcription	NHEK	skin
42	chr6:29569000-29582600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr6:29569000-29582800	Strong transcription	Osteobl	bone
44	chr6:29569000-29584600	Strong transcription	Spleen	Spleen
45	chr6:29569000-29592400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:29569200-29571800	Strong transcription	Brain Anterior Caudate	brain
47	chr6:29569200-29571800	Weak transcription	Gastric	stomach
48	chr6:29569200-29572200	Weak transcription	Fetal Intestine Small	intestine
49	chr6:29569200-29572600	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr6:29569200-29582800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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