Variant report

Variant	esv1851896
Chromosome Location	chr6:31230800-31238694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:855)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:31235265-31236206	GM12878	blood:	n/a	n/a
2	ATF2	chr6:31234577-31234827	GM12878	blood:	n/a	n/a
3	ATF2	chr6:31235142-31236449	GM12878	blood:	n/a	n/a
4	BCL11A	chr6:31234485-31235770	GM12878	blood:	n/a	n/a
5	BCL3	chr6:31235264-31235791	GM12878	blood:	n/a	n/a
6	BCL3	chr6:31235297-31235807	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:31235169-31236336	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:31234491-31234960	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:31235268-31236420	GM12878	blood:	n/a	n/a
10	CEBPB	chr6:31238263-31238458	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:31238283-31238347	HepG2	liver:	n/a	n/a
12	CHD2	chr6:31236281-31236435	GM12878	blood:	n/a	n/a
13	CHD2	chr6:31235463-31235965	GM12878	blood:	n/a	n/a
14	CTCF	chr6:31236393-31236406	GM20000	blood:	n/a	n/a
15	EBF1	chr6:31238174-31238454	GM12878	blood:	n/a	chr6:31238300-31238311
16	EGR1	chr6:31235592-31235729	GM12878	blood:	n/a	n/a
17	ELF1	chr6:31235168-31235782	GM12878	blood:	n/a	n/a
18	FOXM1	chr6:31234918-31235825	GM12878	blood:	n/a	n/a
19	FOXM1	chr6:31235297-31236252	GM12878	blood:	n/a	n/a
20	KAP1	chr6:31231259-31231678	K562	blood:	n/a	n/a
21	KAP1	chr6:31231183-31231702	HEK293	kidney:	n/a	n/a
22	KAP1	chr6:31235780-31236308	HEK293	kidney:	n/a	chr6:31236056-31236064
23	MAX	chr6:31231172-31231364	NB4	blood:	n/a	n/a
24	MTA3	chr6:31234625-31234973	GM12878	blood:	n/a	n/a
25	MTA3	chr6:31238088-31239031	GM12878	blood:	n/a	n/a
26	MTA3	chr6:31234400-31236514	GM12878	blood:	n/a	n/a
27	MTA3	chr6:31235131-31236155	GM12878	blood:	n/a	n/a
28	NFATC1	chr6:31236775-31237485	GM12878	blood:	n/a	n/a
29	NFATC1	chr6:31234445-31236347	GM12878	blood:	n/a	n/a
30	NFATC1	chr6:31234498-31236222	GM12878	blood:	n/a	n/a
31	NFIC	chr6:31234556-31235054	GM12878	blood:	n/a	n/a
32	NFIC	chr6:31235262-31236277	GM12878	blood:	n/a	n/a
33	PAX5	chr6:31238042-31238247	GM12878	blood:	n/a	n/a
34	PAX5	chr6:31234747-31235373	GM12878	blood:	n/a	n/a
35	PBX3	chr6:31234582-31234746	GM12878	blood:	n/a	n/a
36	PBX3	chr6:31234539-31234724	GM12878	blood:	n/a	n/a
37	PBX3	chr6:31234844-31235179	GM12878	blood:	n/a	n/a
38	PBX3	chr6:31234963-31235089	GM12878	blood:	n/a	n/a
39	PML	chr6:31235215-31236239	GM12878	blood:	n/a	chr6:31236056-31236064
40	PML	chr6:31234448-31236731	GM12878	blood:	n/a	chr6:31236056-31236064
41	POLR2A	chr6:31236101-31236572	GM12878	blood:	n/a	n/a
42	POLR2A	chr6:31235261-31235952	U87	brain:	n/a	n/a
43	POLR2A	chr6:31236914-31238218	GM12878	blood:	n/a	n/a
44	POLR2A	chr6:31234623-31236514	GM18526	blood:	n/a	n/a
45	POLR2A	chr6:31235590-31236101	HCT-116	colon:	n/a	n/a
46	POLR2A	chr6:31235906-31235924	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr6:31237761-31237969	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr6:31236948-31237097	HepG2	liver:	n/a	n/a
49	POLR2A	chr6:31235283-31235951	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr6:31233203-31241373	GM12892	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31237824-31237874	H1-hESC	embryonic stem cell:	embryo
2	chr6:31237824-31237874	H1-hESC	embryonic stem cell:	embryo
3	chr6:31237013-31237063	ovcar-3	ovarian:	n/a
4	chr6:31237824-31237874	HUVEC	blood vessel:	n/a
5	chr6:31238245-31238295	SK-N-SH	brain:	n/a
6	chr6:31238036-31238086	AG09319	gingival:	n/a
7	chr6:31237013-31237063	ECC-1	luminal epithelium:	n/a
8	chr6:31237664-31237714	ECC-1	luminal epithelium:	n/a
9	chr6:31238245-31238295	HCPEpiC	choroid plexus:	n/a
10	chr6:31237013-31237063	PANC-1	pancreas:	n/a
11	chr6:31237199-31237249	AG09309	skin:	n/a
12	chr6:31237029-31237079	SKMC	muscle:	n/a
13	chr6:31237013-31237063	BE2_C	brain:	n/a
14	chr6:31237034-31237084	U87	brain:	n/a
15	chr6:31237034-31237084	AG04449	skin:	fetal
16	chr6:31238020-31238070	NHBE	bronchial:	n/a
17	chr6:31237034-31237084	GM06990	blood:	n/a
18	chr6:31237824-31237874	SK-N-SH_RA	brain:	n/a
19	chr6:31237034-31237084	SKMC	muscle:	n/a
20	chr6:31237013-31237063	HL-60	blood:	n/a
21	chr6:31237405-31237455	Hepatocyte	liver:	n/a
22	chr6:31235956-31236006	ECC-1	luminal epithelium:	n/a
23	chr6:31237029-31237079	K562	blood:	n/a
24	chr6:31237034-31237084	NB4	blood:	n/a
25	chr6:31238036-31238086	AG09309	skin:	n/a
26	chr6:31238388-31238438	MCF-7	breast:	n/a
27	chr6:31238020-31238070	H1-hESC	embryonic stem cell:	embryo
28	chr6:31237824-31237874	HMEC	breast:	n/a
29	chr6:31238388-31238438	RPTEC	kidney:	n/a
30	chr6:31238020-31238070	A549	lung:	n/a
31	chr6:31238020-31238070	HCF	heart:	n/a
32	chr6:31237199-31237249	HCM	heart:	n/a
33	chr6:31238036-31238086	MCF10A-Er-Src	breast:	n/a
34	chr6:31238020-31238070	HRPEpiC	eye:	n/a
35	chr6:31237664-31237714	GM12878	blood:	n/a
36	chr6:31238388-31238438	AG04450	lung:	fetal
37	chr6:31237722-31237772	CMK	blood:	n/a
38	chr6:31238267-31238317	HEEpiC	esophagus:	n/a
39	chr6:31237405-31237455	AG04449	skin:	fetal
40	chr6:31237664-31237714	GM12892	blood:	n/a
41	chr6:31237664-31237714	SK-N-MC	brain:	n/a
42	chr6:31237405-31237455	NHBE	bronchial:	n/a
43	chr6:31238036-31238086	GM12878	blood:	n/a
44	chr6:31235956-31236006	GM12878	blood:	n/a
45	chr6:31238388-31238438	HCF	heart:	n/a
46	chr6:31237034-31237084	NHBE	bronchial:	n/a
47	chr6:31235956-31236006	GM19239	blood:	n/a
48	chr6:31237034-31237084	RPTEC	kidney:	n/a
49	chr6:31238388-31238438	Jurkat	blood:	n/a
50	chr6:31238245-31238295	ProgFib	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
2	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
3	chr6:31234807..31237311-chr6:31237898..31240961,3	K562	blood:
4	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
5	chr6:31176797..31178729-chr6:31234671..31236847,2	K562	blood:
6	chr6:31235298..31236799-chr6:31321704..31323597,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-2	chr6:31236531-31236950	NONHSAT108747
2	lnc-HLA-C-2	chr6:31236526-31236950	NONHSAT108746
3	lnc-HLA-C-2	chr6:31237115-31237443	NONHSAT108746

No data

Variant related genes	Relation type
USP8P1	TF binding region
HLA-C	TF binding region
USP8P1	CpG island
HLA-C	CpG island
ENSG00000234745	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000271581	chromatin interactions

Extended variants
information (count: 762 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2245822	chr6:31230800-31230801	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114846427	chr6:31230805-31230806	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs530397908	chr6:31230821-31230822	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs564050496	chr6:31230822-31230823	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs183757515	chr6:31230823-31230824	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs113288069	chr6:31230833-31230834	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs2524117	chr6:31230869-31230870	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs373321660	chr6:31230870-31230871	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs375773372	chr6:31230872-31230873	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs2394952	chr6:31230882-31230883	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs571220554	chr6:31230893-31230894	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs7747738	chr6:31230924-31230925	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs553662783	chr6:31230975-31230976	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs2894198	chr6:31230990-31230991	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs570531345	chr6:31231015-31231016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9264440	chr6:31231019-31231020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs80244499	chr6:31231036-31231037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9264441	chr6:31231068-31231069	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs565299253	chr6:31231073-31231074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138208907	chr6:31231078-31231079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549791372	chr6:31231082-31231083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186640535	chr6:31231085-31231086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9264442	chr6:31231097-31231098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9264443	chr6:31231105-31231106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2853962	chr6:31231106-31231107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9264445	chr6:31231114-31231115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549481963	chr6:31231115-31231116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9264446	chr6:31231117-31231118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs9264447	chr6:31231130-31231131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs547508069	chr6:31231136-31231137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9264448	chr6:31231142-31231143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs150198053	chr6:31231164-31231165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2524116	chr6:31231176-31231177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs112761503	chr6:31231182-31231183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372554401	chr6:31231192-31231193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9264450	chr6:31231193-31231194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs9264451	chr6:31231199-31231200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs577203210	chr6:31231211-31231212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74789993	chr6:31231219-31231220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375151418	chr6:31231232-31231233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9264453	chr6:31231234-31231235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs9501555	chr6:31231245-31231246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563894402	chr6:31231262-31231263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9501556	chr6:31231268-31231269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546510144	chr6:31231299-31231300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146109832	chr6:31231300-31231301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140183498	chr6:31231301-31231302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9501557	chr6:31231306-31231307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs78595379	chr6:31231312-31231313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569636411	chr6:31231320-31231321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
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
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Ovarian cancer	21781307	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
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	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
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31228200-31235800	Weak transcription	Fetal Thymus	thymus
2	chr6:31228400-31233800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr6:31228400-31235400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr6:31228600-31234800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr6:31230200-31235600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:31230600-31230800	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
7	chr6:31230600-31231000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
8	chr6:31231000-31234600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr6:31231800-31235600	Weak transcription	Left Ventricle	heart
10	chr6:31232400-31235400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:31232600-31235600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:31232600-31236800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:31232800-31235600	Weak transcription	Colonic Mucosa	Colon
14	chr6:31232800-31235800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:31233000-31235200	Weak transcription	Primary T cells from cord blood	blood
16	chr6:31233000-31235400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:31233200-31235600	Weak transcription	Liver	Liver
18	chr6:31233200-31235800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:31233200-31235800	Weak transcription	Placenta	Placenta
20	chr6:31233200-31236000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:31233200-31236600	Weak transcription	HMEC	breast
22	chr6:31233200-31238200	Weak transcription	Stomach Mucosa	stomach
23	chr6:31233200-31238400	Weak transcription	Small Intestine	intestine
24	chr6:31233400-31233600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:31233400-31234400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr6:31233400-31235400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:31233400-31235600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr6:31233400-31235800	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr6:31233400-31235800	Weak transcription	Adipose Nuclei	Adipose
30	chr6:31233400-31235800	Weak transcription	GM12878-XiMat	blood
31	chr6:31233400-31236200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:31233600-31235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:31233600-31236400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:31233800-31234000	Enhancers	Primary B cells from cord blood	blood
35	chr6:31233800-31234000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr6:31233800-31235400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:31233800-31236000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:31233800-31236400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:31233800-31236600	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:31233800-31236800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr6:31234000-31234200	Weak transcription	Spleen	Spleen
42	chr6:31234000-31234600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr6:31234000-31235400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:31234000-31235400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr6:31234000-31235600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:31234000-31235800	Weak transcription	Esophagus	oesophagus
47	chr6:31234000-31235800	Weak transcription	Gastric	stomach
48	chr6:31234000-31236000	Weak transcription	Primary B cells from cord blood	blood
49	chr6:31234000-31236200	Weak transcription	Aorta	Aorta
50	chr6:31234000-31236800	Weak transcription	Rectal Smooth Muscle	rectum

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