Variant report

Variant	nsv886637
Chromosome Location	chr6:126927717-126985351
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	CBX3	chr6:126976164-126976425	K562	blood:	n/a	n/a
2	CEBPB	chr6:126982864-126983265	IMR90	lung:	n/a	n/a
3	CEBPB	chr6:126962895-126963216	HepG2	liver:	n/a	chr6:126962898-126962911 chr6:126963134-126963147 chr6:126963134-126963147 chr6:126963062-126963073 chr6:126963136-126963147
4	CEBPB	chr6:126962962-126963184	A549	lung:	n/a	chr6:126963134-126963147 chr6:126963134-126963147 chr6:126963062-126963073 chr6:126963136-126963147
5	CEBPB	chr6:126952650-126952914	HepG2	liver:	n/a	chr6:126952769-126952780 chr6:126952769-126952782
6	CEBPB	chr6:126971437-126971786	HepG2	liver:	n/a	chr6:126971589-126971600
7	CEBPB	chr6:126962922-126963198	IMR90	lung:	n/a	chr6:126963134-126963147 chr6:126963134-126963147 chr6:126963062-126963073 chr6:126963136-126963147
8	CTCF	chr6:126978771-126979017	Hela-S3	cervix:	n/a	chr6:126978890-126978908
9	CTCF	chr6:126978820-126978970	AG10803	skin:	n/a	chr6:126978890-126978908
10	CTCF	chr6:126978820-126978970	HBMEC	blood vessel:	n/a	chr6:126978890-126978908
11	CTCF	chr6:126949540-126949690	HCT-116	colon:	n/a	n/a
12	CTCF	chr6:126984480-126984630	MCF-7	breast:	n/a	n/a
13	CTCF	chr6:126949460-126949610	GM12872	blood:	n/a	chr6:126949503-126949524
14	CTCF	chr6:126978840-126978990	GM06990	blood:	n/a	chr6:126978890-126978908
15	CTCF	chr6:126949400-126949550	GM12865	blood:	n/a	chr6:126949503-126949524
16	CTCF	chr6:126978840-126978990	GM12872	blood:	n/a	chr6:126978890-126978908
17	CTCF	chr6:126953100-126953250	AG10803	skin:	n/a	n/a
18	CTCF	chr6:126949440-126949590	GM12870	blood:	n/a	chr6:126949503-126949524
19	CTCF	chr6:126978873-126978932	A549	lung:	n/a	chr6:126978890-126978908
20	CTCF	chr6:126949380-126949530	HCT-116	colon:	n/a	chr6:126949503-126949524
21	CTCF	chr6:126949440-126949590	GM12866	blood:	n/a	chr6:126949503-126949524
22	CTCF	chr6:126949400-126949550	GM12867	blood:	n/a	chr6:126949503-126949524
23	CTCF	chr6:126984600-126984750	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr6:126978780-126978930	GM12873	blood:	n/a	chr6:126978890-126978908
25	CTCF	chr6:126978759-126978978	HepG2	liver:	n/a	chr6:126978890-126978908
26	CTCF	chr6:126978863-126978956	Spleen_OC	spleen:	n/a	chr6:126978890-126978908
27	CTCF	chr6:126949407-126949565	GM19238	blood:	n/a	chr6:126949503-126949524
28	CTCF	chr6:126978811-126979000	GM10248	blood:	n/a	chr6:126978890-126978908
29	CTCF	chr6:126984660-126984810	RPTEC	kidney:	n/a	n/a
30	CTCF	chr6:126984640-126984790	HMF	breast:	n/a	n/a
31	CTCF	chr6:126978840-126978990	BE2_C	brain:	n/a	chr6:126978890-126978908
32	CTCF	chr6:126978790-126979005	Pancreas_OC	pancreas:	n/a	chr6:126978890-126978908
33	CTCF	chr6:126973320-126973470	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr6:126949380-126949530	SAEC	small airway:	n/a	chr6:126949503-126949524
35	CTCF	chr6:126973360-126973510	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr6:126949360-126949510	GM12874	blood:	n/a	n/a
37	CTCF	chr6:126978840-126978990	SK-N-SH_RA	brain:	n/a	chr6:126978890-126978908
38	CTCF	chr6:126973240-126973390	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:126984540-126984690	NHEK	skin:	n/a	n/a
40	CTCF	chr6:126978740-126978890	HAc	cerebellar:	n/a	n/a
41	CTCF	chr6:126978820-126978970	GM12866	blood:	n/a	chr6:126978890-126978908
42	CTCF	chr6:126949380-126949530	HA-sp	spinal cord:	n/a	chr6:126949503-126949524
43	CTCF	chr6:126973260-126973410	GM12873	blood:	n/a	n/a
44	CTCF	chr6:126949440-126949590	GM12864	blood:	n/a	chr6:126949503-126949524
45	CTCF	chr6:126978790-126979006	MCF-7	breast:	n/a	chr6:126978890-126978908
46	CTCF	chr6:126973240-126973390	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr6:126978840-126978990	HA-sp	spinal cord:	n/a	chr6:126978890-126978908
48	CTCF	chr6:126949780-126949930	GM12865	blood:	n/a	n/a
49	CTCF	chr6:126978800-126978950	GM12865	blood:	n/a	chr6:126978890-126978908
50	CTCF	chr6:126973220-126973370	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:126964983-126965033	AoSMC	blood vessel:	n/a
2	chr6:126964727-126964777	A549	lung:	n/a
3	chr6:126964983-126965033	AoSMC	blood vessel:	n/a
4	chr6:126964727-126964777	A549	lung:	n/a
5	chr6:126964945-126964995	T-47D	breast:	n/a
6	chr6:126964499-126964549	A549	lung:	n/a
7	chr6:126964983-126965033	SKMC	muscle:	n/a
8	chr6:126964779-126964829	Hela-S3	cervix:	n/a
9	chr6:126965162-126965212	GM19239	blood:	n/a
10	chr6:126964983-126965033	HRPEpiC	eye:	n/a
11	chr6:126964983-126965033	HCPEpiC	choroid plexus:	n/a
12	chr6:126964945-126964995	GM12891	blood:	n/a
13	chr6:126964945-126964995	K562	blood:	n/a
14	chr6:126967348-126967398	HCF	heart:	n/a
15	chr6:126964779-126964829	HRPEpiC	eye:	n/a
16	chr6:126964945-126964995	HNPCEpiC	eye:	n/a
17	chr6:126964983-126965033	HCF	heart:	n/a
18	chr6:126964983-126965033	HAEpiC	amniotic membrane:	n/a
19	chr6:126964727-126964777	HRCEpiC	kidney:	n/a
20	chr6:126984891-126984941	ovcar-3	ovarian:	n/a
21	chr6:126964779-126964829	GM06990	blood:	n/a
22	chr6:126964983-126965033	NB4	blood:	n/a
23	chr6:126967348-126967398	HCPEpiC	choroid plexus:	n/a
24	chr6:126984891-126984941	GM12891	blood:	n/a
25	chr6:126984891-126984941	SK-N-SH_RA	brain:	n/a
26	chr6:126964945-126964995	PFSK-1	brain:	n/a
27	chr6:126964499-126964549	SAEC	small airway:	n/a
28	chr6:126984891-126984941	SKMC	muscle:	n/a
29	chr6:126984891-126984941	HCPEpiC	choroid plexus:	n/a
30	chr6:126984891-126984941	MCF10A-Er-Src	breast:	n/a
31	chr6:126964779-126964829	A549	lung:	n/a
32	chr6:126967348-126967398	HNPCEpiC	eye:	n/a
33	chr6:126984891-126984941	NHDF-neo	bronchial:	n/a
34	chr6:126964945-126964995	AG04449	skin:	fetal
35	chr6:126964499-126964549	NHBE	bronchial:	n/a
36	chr6:126965162-126965212	HepG2	liver:	n/a
37	chr6:126965162-126965212	HMEC	breast:	n/a
38	chr6:126964727-126964777	PrEC	prostate:	n/a
39	chr6:126964727-126964777	GM12891	blood:	n/a
40	chr6:126964499-126964549	HUVEC	blood vessel:	n/a
41	chr6:126967348-126967398	MCF10A-Er-Src	breast:	n/a
42	chr6:126984891-126984941	HAEpiC	amniotic membrane:	n/a
43	chr6:126964945-126964995	NT2-D1	testis:	n/a
44	chr6:126965162-126965212	HEK293	kidney:	embryo
45	chr6:126964945-126964995	AG04450	lung:	fetal
46	chr6:126964779-126964829	RPTEC	kidney:	n/a
47	chr6:126984891-126984941	ECC-1	luminal epithelium:	n/a
48	chr6:126964945-126964995	HCM	heart:	n/a
49	chr6:126964983-126965033	PFSK-1	brain:	n/a
50	chr6:126964779-126964829	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:126681352..126682819-chr6:126978200..126979711,9	MCF-7	breast:
2	chr6:126978877..126980951-chr6:126980996..126982518,2	K562	blood:
3	chr6:126104351..126106152-chr6:126976886..126978801,2	K562	blood:
4	chr6:126978877..126980951-chr6:126980996..126982518,2	K562	blood:
5	chr6:126950096..126952625-chr6:126952673..126954868,2	K562	blood:
6	chr6:126972073..126973820-chr6:126977555..126980323,2	K562	blood:
7	chr6:126497226..126499116-chr6:126978398..126980565,2	MCF-7	breast:
8	chr6:126964408..126966689-chr6:126968469..126970868,2	K562	blood:
9	chr6:126682058..126683013-chr6:126978432..126979264,4	MCF-7	breast:
10	chr6:126950096..126952625-chr6:126952673..126954868,2	K562	blood:
11	chr6:126972073..126973820-chr6:126977555..126980323,2	K562	blood:

Variant related genes	Relation type
VIMP1	TF binding region
PRELID1P1	TF binding region
VIMP1	CpG island
PRELID1P1	CpG island
ENSG00000231842	chromatin interactions
ENSG00000217325	chromatin interactions

Extended variants
information (count: 983 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540146993	chr6:126929254-126929255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565471185	chr6:126929342-126929343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577429883	chr6:126929350-126929351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544500705	chr6:126929361-126929362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563024003	chr6:126929400-126929401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530630994	chr6:126929422-126929423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556464732	chr6:126929432-126929433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561393623	chr6:126929453-126929454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549138129	chr6:126929532-126929533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151017123	chr6:126929538-126929539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73773104	chr6:126929545-126929546	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546562219	chr6:126929599-126929600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140825904	chr6:126929600-126929601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188995859	chr6:126929705-126929706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193130491	chr6:126929709-126929710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550506639	chr6:126929722-126929723	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs568671643	chr6:126929754-126929755	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs35314048	chr6:126929768-126929769	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs536030804	chr6:126929781-126929782	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs117191969	chr6:126929796-126929797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552706357	chr6:126935608-126935609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538445158	chr6:126935617-126935618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557062405	chr6:126935640-126935641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575320282	chr6:126935663-126935664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7738270	chr6:126935664-126935665	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs12208713	chr6:126935671-126935672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142985445	chr6:126935672-126935673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573463679	chr6:126935755-126935756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185139885	chr6:126935763-126935764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374128739	chr6:126935812-126935813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552598779	chr6:126935838-126935839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376071001	chr6:126935855-126935856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565432900	chr6:126935862-126935863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75839965	chr6:126935939-126935940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544802125	chr6:126935940-126935941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563386761	chr6:126935953-126935954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530593178	chr6:126936037-126936038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569491516	chr6:126936038-126936039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560900371	chr6:126936121-126936122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528064950	chr6:126936132-126936133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370653070	chr6:126936137-126936138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546922063	chr6:126936195-126936196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377314510	chr6:126936212-126936213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571429936	chr6:126936214-126936215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7738836	chr6:126936235-126936236	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs370100901	chr6:126936240-126936241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71272314	chr6:126936254-126936255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550327786	chr6:126936260-126936261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190023860	chr6:126936267-126936268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373672553	chr6:126936279-126936280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	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
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21785460	CNVD
Neurocytoma	17123091	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21958427	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:126929200-126929600	Enhancers	Fetal Brain Female	brain
2	chr6:126929200-126929600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr6:126929400-126929800	Enhancers	Fetal Brain Male	brain
4	chr6:126935600-126936600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr6:126935600-126936800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:126935800-126936200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:126935800-126936200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr6:126936000-126936400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:126936000-126936600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:126936000-126936600	Enhancers	Colonic Mucosa	Colon
11	chr6:126936200-126936600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr6:126936200-126939400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr6:126937800-126938200	Enhancers	Fetal Brain Female	brain
14	chr6:126937800-126938400	Enhancers	Fetal Brain Male	brain
15	chr6:126939400-126940000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr6:126939600-126940200	Enhancers	Fetal Intestine Small	intestine
17	chr6:126939600-126940400	Enhancers	Fetal Intestine Large	intestine
18	chr6:126940000-126940200	Enhancers	Fetal Brain Female	brain
19	chr6:126940000-126940200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr6:126940200-126940400	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr6:126948200-126948800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:126948800-126949200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:126949200-126950000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:126950600-126950800	Enhancers	Fetal Brain Male	brain
25	chr6:126950800-126952800	Weak transcription	Fetal Brain Male	brain
26	chr6:126951600-126955000	Enhancers	NHDF-Ad	bronchial
27	chr6:126952200-126953000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:126952400-126953600	Enhancers	Colon Smooth Muscle	Colon
29	chr6:126952600-126953200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:126952800-126953400	Enhancers	Fetal Brain Male	brain
31	chr6:126952800-126955200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:126953000-126953200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:126953000-126953400	Enhancers	Fetal Kidney	kidney
34	chr6:126953000-126953400	Enhancers	Fetal Lung	lung
35	chr6:126953200-126953400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:126953200-126953400	Enhancers	Rectal Smooth Muscle	rectum
37	chr6:126953200-126953600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr6:126953400-126953600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:126953400-126954400	Weak transcription	Fetal Lung	lung
40	chr6:126953400-126954400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr6:126953600-126954400	Weak transcription	Colon Smooth Muscle	Colon
42	chr6:126953600-126955000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:126953600-126955200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:126954200-126954600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr6:126954200-126954800	Enhancers	Fetal Stomach	stomach
46	chr6:126954200-126954800	Enhancers	Stomach Smooth Muscle	stomach
47	chr6:126954400-126954800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:126954400-126954800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:126954400-126954800	Enhancers	Colon Smooth Muscle	Colon
50	chr6:126954400-126954800	Enhancers	Rectal Smooth Muscle	rectum

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