Variant report

Variant	esv3399875
Chromosome Location	chr6:31602167-31602530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:31602520-31602670	HUVEC	blood vessel:	n/a	n/a
2	CTCF	chr6:31602500-31602650	AG09309	skin:	n/a	n/a
3	CTCF	chr6:31602480-31602630	GM12871	blood:	n/a	n/a
4	CTCF	chr6:31602480-31602630	Caco-2	colon:	n/a	n/a
5	CTCF	chr6:31602500-31602650	HBMEC	blood vessel:	n/a	n/a
6	CTCF	chr6:31602520-31602670	GM12871	blood:	n/a	n/a
7	CTCF	chr6:31602500-31602650	HFF	foreskin:	n/a	n/a
8	CTCF	chr6:31602515-31602663	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr6:31602500-31602650	GM12873	blood:	n/a	n/a
10	CTCF	chr6:31602480-31602630	HRE	kidney:	n/a	n/a
11	CTCF	chr6:31602480-31602630	HEK293	kidney:	n/a	n/a
12	CTCF	chr6:31602450-31602761	K562	blood:	n/a	n/a
13	CTCF	chr6:31602420-31602570	BE2_C	brain:	n/a	n/a
14	CTCF	chr6:31602500-31602650	NB4	blood:	n/a	n/a
15	CTCF	chr6:31602520-31602670	GM12873	blood:	n/a	n/a
16	CTCF	chr6:31602460-31602610	GM12878	blood:	n/a	n/a
17	CTCF	chr6:31602500-31602650	BJ	skin:	n/a	n/a
18	CTCF	chr6:31602500-31602650	GM06990	blood:	n/a	n/a
19	CTCF	chr6:31602420-31602570	WERI-Rb-1	eye:	n/a	n/a
20	POLR2A	chr6:31599299-31602572	HepG2	liver:	n/a	n/a
21	POLR2A	chr6:31599397-31603482	HepG2	liver:	n/a	n/a
22	POLR2A	chr6:31597439-31602680	PANC-1	pancreas:	n/a	n/a
23	POLR2A	chr6:31601834-31603572	K562	blood:	n/a	n/a
24	POLR2A	chr6:31597463-31604060	GM12892	blood:	n/a	n/a
25	POLR2A	chr6:31597554-31603876	K562	blood:	n/a	n/a
26	POLR2A	chr6:31602158-31602732	GM12878	blood:	n/a	n/a
27	POLR2A	chr6:31602238-31602787	HL-60	blood:	n/a	n/a
28	POLR2A	chr6:31602394-31602478	GM12878	blood:	n/a	n/a
29	POLR2A	chr6:31602416-31602611	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr6:31602061-31603550	GM12891	blood:	n/a	n/a
31	POLR2A	chr6:31601781-31602472	GM12878	blood:	n/a	n/a
32	POLR2A	chr6:31601947-31603333	K562	blood:	n/a	n/a
33	POLR2A	chr6:31598920-31603651	GM12891	blood:	n/a	n/a
34	POLR2A	chr6:31601802-31602200	SK-N-SH	brain:	n/a	n/a
35	POLR2A	chr6:31602429-31602610	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr6:31602026-31604476	GM12892	blood:	n/a	n/a
37	POLR2A	chr6:31602105-31602799	MCF-7	breast:	n/a	n/a
38	POLR2A	chr6:31601004-31602449	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr6:31600977-31602423	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr6:31602129-31602430	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr6:31592721-31608143	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr6:31602508-31602698	GM12878	blood:	n/a	n/a
43	POLR2A	chr6:31596182-31603913	PFSK-1	brain:	n/a	n/a
44	POLR2A	chr6:31602218-31602716	GM12878	blood:	n/a	n/a
45	POLR2A	chr6:31602206-31602552	A549	lung:	n/a	n/a
46	POLR2A	chr6:31601838-31602190	HCT-116	colon:	n/a	n/a
47	POLR2A	chr6:31602476-31603491	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr6:31592751-31609100	GM12878	blood:	n/a	n/a
49	POLR2A	chr6:31601696-31602597	GM12892	blood:	n/a	n/a
50	POLR2A	chr6:31602085-31602847	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31602269-31602319	GM19239	blood:	n/a
2	chr6:31602269-31602319	GM12891	blood:	n/a
3	chr6:31602130-31602180	AG04450	lung:	fetal
4	chr6:31602130-31602180	SK-N-MC	brain:	n/a
5	chr6:31602130-31602180	H1-hESC	embryonic stem cell:	embryo
6	chr6:31602130-31602180	NHBE	bronchial:	n/a
7	chr6:31602269-31602319	K562	blood:	n/a
8	chr6:31602257-31602307	NHDF-neo	bronchial:	n/a
9	chr6:31602269-31602319	HUVEC	blood vessel:	n/a
10	chr6:31602130-31602180	AoSMC	blood vessel:	n/a
11	chr6:31602257-31602307	PANC-1	pancreas:	n/a
12	chr6:31602257-31602307	PFSK-1	brain:	n/a
13	chr6:31602130-31602180	BJ	skin:	n/a
14	chr6:31602130-31602180	SKMC	muscle:	n/a
15	chr6:31602269-31602319	GM06990	blood:	n/a
16	chr6:31602257-31602307	HIPEpiC	eye:	n/a
17	chr6:31602269-31602319	Hela-S3	cervix:	n/a
18	chr6:31602269-31602319	HCT-116	colon:	n/a
19	chr6:31602269-31602319	SKMC	muscle:	n/a
20	chr6:31602269-31602319	MCF-7	breast:	n/a
21	chr6:31602130-31602180	GM19239	blood:	n/a
22	chr6:31602257-31602307	SK-N-SH	brain:	n/a
23	chr6:31602257-31602307	HEK293	kidney:	embryo
24	chr6:31602269-31602319	IMR90	lung:	fetal
25	chr6:31602269-31602319	AG09319	gingival:	n/a
26	chr6:31602130-31602180	NHDF-neo	bronchial:	n/a
27	chr6:31602269-31602319	MCF10A-Er-Src	breast:	n/a
28	chr6:31602257-31602307	SAEC	small airway:	n/a
29	chr6:31602130-31602180	HAEpiC	amniotic membrane:	n/a
30	chr6:31602130-31602180	SK-N-SH	brain:	n/a
31	chr6:31602269-31602319	Hepatocyte	liver:	n/a
32	chr6:31602257-31602307	CMK	blood:	n/a
33	chr6:31602257-31602307	AG09309	skin:	n/a
34	chr6:31602257-31602307	HRE	kidney:	n/a
35	chr6:31602130-31602180	Hela-S3	cervix:	n/a
36	chr6:31602269-31602319	ECC-1	luminal epithelium:	n/a
37	chr6:31602257-31602307	AG09319	gingival:	n/a
38	chr6:31602269-31602319	AG04449	skin:	fetal
39	chr6:31602257-31602307	RPTEC	kidney:	n/a
40	chr6:31602257-31602307	AoSMC	blood vessel:	n/a
41	chr6:31602257-31602307	AG10803	skin:	n/a
42	chr6:31602257-31602307	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:31602269-31602319	HRE	kidney:	n/a
44	chr6:31602269-31602319	HL-60	blood:	n/a
45	chr6:31602130-31602180	LNCaP	prostate:	n/a
46	chr6:31602257-31602307	HRCEpiC	kidney:	n/a
47	chr6:31602130-31602180	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:31602269-31602319	BJ	skin:	n/a
49	chr6:31602257-31602307	Caco-2	colon:	n/a
50	chr6:31602269-31602319	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31513227..31514963-chr6:31602419..31605642,3	K562	blood:
2	chr6:31507082..31510843-chr6:31599707..31603450,4	K562	blood:
3	chr6:31601006..31603975-chr6:31604040..31605763,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRRC2A	TF binding region
PRRC2A	CpG island
ENSG00000234006	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000204498	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000254870	chromatin interactions
ENSG00000213760	chromatin interactions
ENSG00000204469	chromatin interactions

Extended variants
information (count: 18 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372189408	chr6:31602169-31602170	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs374880749	chr6:31602214-31602215	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs142164582	chr6:31602219-31602220	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs115932182	chr6:31602256-31602257	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs199623123	chr6:31602258-31602259	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs267600958	chr6:31602268-31602269	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs267600959	chr6:31602269-31602270	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs145948939	chr6:31602270-31602271	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs115992473	chr6:31602295-31602296	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs547482834	chr6:31602366-31602367	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs371338060	chr6:31602377-31602378	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs147002415	chr6:31602388-31602389	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs368847439	chr6:31602396-31602397	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs147671125	chr6:31602398-31602399	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs547347098	chr6:31602445-31602446	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs537764148	chr6:31602466-31602467	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs375305163	chr6:31602480-31602481	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs2242657	chr6:31602489-31602490	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:131)

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	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
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31589800-31619400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:31590200-31607000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr6:31590200-31617600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:31590200-31618800	Strong transcription	Primary B cells from peripheral blood	blood
5	chr6:31590400-31617400	Strong transcription	Rectal Smooth Muscle	rectum
6	chr6:31590400-31617600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr6:31590400-31618200	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr6:31590400-31618600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr6:31590400-31618600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:31590400-31618600	Strong transcription	Fetal Intestine Small	intestine
11	chr6:31590600-31605000	Strong transcription	A549	lung
12	chr6:31590600-31605200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr6:31590600-31606200	Strong transcription	Primary hematopoietic stem cells	blood
14	chr6:31590600-31613200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:31590600-31617200	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr6:31590600-31617400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:31590600-31617400	Strong transcription	Right Ventricle	heart
18	chr6:31590600-31617600	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:31590600-31617800	Strong transcription	H9 Cell Line	embryonic stem cell
20	chr6:31590600-31617800	Strong transcription	Left Ventricle	heart
21	chr6:31590600-31617800	Strong transcription	Thymus	Thymus
22	chr6:31590600-31618000	Strong transcription	Fetal Lung	lung
23	chr6:31590600-31618600	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr6:31590600-31618600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:31590600-31618800	Strong transcription	Fetal Stomach	stomach
26	chr6:31590800-31602200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:31590800-31604600	Strong transcription	Fetal Muscle Leg	muscle
28	chr6:31590800-31605600	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr6:31590800-31607000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:31590800-31607000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:31590800-31607200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:31590800-31609200	Strong transcription	Brain Anterior Caudate	brain
33	chr6:31590800-31617400	Strong transcription	Stomach Smooth Muscle	stomach
34	chr6:31590800-31617600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:31590800-31617800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:31590800-31617800	Strong transcription	Duodenum Mucosa	Duodenum
37	chr6:31590800-31618400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:31590800-31618400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:31590800-31618600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:31590800-31618600	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:31590800-31618600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr6:31590800-31618600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr6:31590800-31618800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:31590800-31619000	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:31591000-31604600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr6:31591000-31604800	Strong transcription	K562	blood
47	chr6:31591000-31605600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
48	chr6:31591000-31607000	Strong transcription	NH-A	brain
49	chr6:31591000-31607000	Strong transcription	Osteobl	bone
50	chr6:31591000-31607200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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