Variant report

Variant	nsv1019561
Chromosome Location	chr6:45485826-45535222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:75)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:24)

No data

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:45492484..45494517-chr6:45500925..45504439,3	MCF-7	breast:
2	chr6:45533105..45535281-chr6:45537536..45540429,2	MCF-7	breast:
3	chr6:45506501..45508928-chr6:45515340..45517008,2	MCF-7	breast:
4	chr6:45505637..45508807-chr6:45512620..45514671,3	MCF-7	breast:
5	chr6:45495679..45498360-chr6:45500683..45502256,2	MCF-7	breast:
6	chr6:45521508..45523893-chr6:45680263..45683412,3	MCF-7	breast:
7	chr6:45488190..45490871-chr6:45499883..45502171,2	K562	blood:
8	chr6:45506501..45508928-chr6:45515340..45517008,2	MCF-7	breast:
9	chr6:45498979..45501523-chr6:45505479..45508098,2	K562	blood:
10	chr6:45533723..45535563-chr6:45552658..45554257,2	MCF-7	breast:
11	chr6:45519509..45521013-chr6:45524867..45526966,2	K562	blood:
12	chr15:40509302..40509813-chr6:45530780..45531300,2	K562	blood:
13	chr6:45490175..45491700-chr6:45519334..45521574,2	MCF-7	breast:
14	chr6:45510384..45512325-chr6:45518225..45520271,2	MCF-7	breast:
15	chr6:45499803..45501981-chr6:45505161..45507219,2	MCF-7	breast:
16	chr6:45519041..45522740-chr6:45522801..45525463,3	MCF-7	breast:
17	chr6:45506661..45509386-chr6:45511675..45515150,3	K562	blood:
18	chr6:45525346..45527240-chr6:45531716..45533270,2	MCF-7	breast:
19	chr6:45517438..45520580-chr6:45520902..45524408,4	MCF-7	breast:
20	chr6:45521858..45524563-chr6:45528701..45531108,3	MCF-7	breast:
21	chr6:45488190..45490871-chr6:45499883..45502171,2	K562	blood:
22	chr6:45483286..45485568-chr6:45489315..45491541,2	K562	blood:
23	chr6:45416687..45419671-chr6:45507233..45509746,2	K562	blood:
24	chr6:45390030..45390535-chr6:45522448..45522980,2	MCF-7	breast:
25	chr6:45343562..45346132-chr6:45499929..45501606,2	K562	blood:
26	chr6:45531563..45533620-chr6:45534711..45536211,2	MCF-7	breast:
27	chr6:45521600..45524007-chr6:45539938..45542034,2	MCF-7	breast:
28	chr6:45519041..45522740-chr6:45522801..45525463,3	MCF-7	breast:
29	chr21:26979413..26980209-chr6:45515504..45516268,2	MCF-7	breast:
30	chr6:45505637..45508807-chr6:45512620..45514671,3	MCF-7	breast:
31	chr6:45514521..45516700-chr6:45519579..45523207,3	MCF-7	breast:
32	chr6:45521062..45522747-chr6:45524709..45527300,2	K562	blood:
33	chr6:45499803..45501981-chr6:45505161..45507219,2	MCF-7	breast:
34	chr6:45490175..45491700-chr6:45519334..45521574,2	MCF-7	breast:
35	chr6:45489161..45491336-chr6:45493728..45495620,2	K562	blood:
36	chr6:45495193..45499204-chr6:45499654..45504200,4	K562	blood:
37	chr6:45507659..45510027-chr6:45511136..45513669,2	K562	blood:
38	chr6:45489161..45491336-chr6:45493728..45495620,2	K562	blood:
39	chr6:45489352..45491036-chr6:45501412..45503775,2	MCF-7	breast:
40	chr6:45504338..45506736-chr6:45575272..45577741,2	MCF-7	breast:
41	chr6:45527779..45529420-chr6:45596792..45598594,2	MCF-7	breast:
42	chr6:45525346..45527240-chr6:45531716..45533270,2	MCF-7	breast:
43	chr6:45507057..45510160-chr6:45510920..45514635,4	MCF-7	breast:
44	chr6:45512077..45515403-chr6:45517360..45519665,3	K562	blood:
45	chr6:45506273..45508464-chr6:45523681..45526573,2	MCF-7	breast:
46	chr6:45388475..45392653-chr6:45521512..45524033,4	MCF-7	breast:
47	chr6:45521062..45522747-chr6:45524709..45527300,2	K562	blood:
48	chr6:45514521..45516700-chr6:45519579..45523207,3	MCF-7	breast:
49	chr6:45498979..45501523-chr6:45505479..45508098,2	K562	blood:
50	chr6:45389098..45392370-chr6:45517089..45519379,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUPT3H-1	chr6:45530215-45530404	XLOC_005737
2	lnc-SUPT3H-1	chr6:45534240-45535428	NONHSAT112988
3	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
4	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
5	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
6	lnc-SUPT3H-1	chr6:45530215-45530404	XLOC_005737
7	lnc-SUPT3H-1	chr6:45523580-45524895	XLOC_005737
8	lnc-SUPT3H-1	chr6:45533740-45534135	XLOC_005737
9	lnc-SUPT3H-1	chr6:45524989-45525046	XLOC_005737
10	lnc-SUPT3H-1	chr6:45535185-45535428	XLOC_005737
11	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
12	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
13	lnc-SUPT3H-1	chr6:45530215-45530404	XLOC_005737
14	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
15	lnc-SUPT3H-1	chr6:45533740-45534135	XLOC_005737
16	lnc-SUPT3H-1	chr6:45530215-45530404	XLOC_005737
17	lnc-SUPT3H-1	chr6:45523580-45524895	XLOC_005737
18	lnc-SUPT3H-1	chr6:45530215-45530404	XLOC_005737
19	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737

No data

(count:24 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RUNX2	hsa-miR-30a-5p	chr6:45515256-45515278
2	RUNX2	hsa-miR-204-5p	chr6:45518681-45518702
3	RUNX2	hsa-miR-433-3p	chr6:45518737-45518758
4	RUNX2	hsa-miR-30d-5p	chr6:45518387-45518408
5	RUNX2	hsa-miR-204-5p	chr6:45518695-45518701
6	RUNX2	hsa-miR-30a-5p	chr6:45518501-45518523
7	RUNX2	hsa-miR-30b-5p	chr6:45518401-45518408
8	RUNX2	hsa-miR-30d-5p	chr6:45518390-45518396
9	RUNX2	hsa-miR-30a-5p	chr6:45518390-45518396
10	RUNX2	hsa-miR-30b-5p	chr6:45518385-45518408
11	RUNX2	hsa-miR-30a-5p	chr6:45518387-45518408
12	RUNX2	hsa-miR-335-5p	chr6:45516005-45516027
13	RUNX2	hsa-miR-30b-5p	chr6:45515256-45515278
14	RUNX2	hsa-miR-155-5p	chr6:45518236-45518256
15	RUNX2	hsa-miR-30d-5p	chr6:45518501-45518523
16	RUNX2	hsa-miR-338-3p	chr6:45516284-45516291
17	RUNX2	hsa-miR-30d-5p	chr6:45518401-45518408
18	RUNX2	hsa-miR-30a-5p	chr6:45518401-45518408
19	RUNX2	hsa-miR-30d-5p	chr6:45515256-45515278
20	RUNX2	hsa-miR-30d-5p	chr6:45518378-45518397
21	RUNX2	hsa-miR-30b-5p	chr6:45518390-45518396
22	RUNX2	hsa-miR-30a-5p	chr6:45518378-45518397
23	RUNX2	hsa-miR-338-3p	chr6:45516272-45516291
24	RUNX2	hsa-miR-204-5p	chr6:45515505-45515528

Variant related genes	Relation type
ENSG00000271857	chromatin interactions
ENSG00000259288	chromatin interactions
ENSG00000154719	chromatin interactions
ENSG00000196284	chromatin interactions
ENSG00000128805	chromatin interactions
ENSG00000124813	chromatin interactions
ENSG00000156970	chromatin interactions
FAM102A	miRNA target sites
ABCC3	miRNA target sites

Extended variants
information (count: 1828 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529770661	chr6:45485861-45485862	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547992021	chr6:45485879-45485880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371477270	chr6:45485907-45485908	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534155001	chr6:45485948-45485949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540797143	chr6:45485966-45485967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559186680	chr6:45485967-45485968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35631485	chr6:45485983-45485984	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570848049	chr6:45486003-45486004	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs181539615	chr6:45486009-45486010	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs200377405	chr6:45486012-45486013	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140860668	chr6:45486015-45486016	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs549431838	chr6:45486025-45486026	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574501075	chr6:45486048-45486049	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186414653	chr6:45486066-45486067	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12665523	chr6:45486103-45486104	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs562888340	chr6:45486116-45486117	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs6916727	chr6:45486117-45486118	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs141828931	chr6:45486135-45486136	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147238008	chr6:45486155-45486156	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139783940	chr6:45486170-45486171	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551794168	chr6:45486183-45486184	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7771889	chr6:45486207-45486208	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563284065	chr6:45486255-45486256	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145275732	chr6:45486312-45486313	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs562430943	chr6:45486332-45486333	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs529674837	chr6:45486333-45486334	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs7754187	chr6:45486383-45486384	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs114399488	chr6:45486431-45486432	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527875249	chr6:45486460-45486461	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs190795393	chr6:45486473-45486474	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs7772562	chr6:45486496-45486497	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs78372878	chr6:45486513-45486514	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs556454451	chr6:45486546-45486547	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs568083920	chr6:45486598-45486599	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182263279	chr6:45486601-45486602	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs554225404	chr6:45486603-45486604	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572488872	chr6:45486609-45486610	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs540420295	chr6:45486628-45486629	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs147193223	chr6:45486756-45486757	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs185940155	chr6:45486774-45486775	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs544485452	chr6:45486897-45486898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs562794970	chr6:45486904-45486905	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs574356772	chr6:45486918-45486919	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541499665	chr6:45486945-45486946	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139567031	chr6:45486959-45486960	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs556008894	chr6:45486982-45486983	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs551864244	chr6:45487039-45487040	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564305544	chr6:45487052-45487053	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116554943	chr6:45487097-45487098	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs550039214	chr6:45487112-45487113	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	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
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	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
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	21510904	CNVD
Cleidocranial dysplasia	20014132	CNVD
Non-small cell lung cancer	17429853	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45465000-45521600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr6:45466800-45488200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:45466800-45497200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:45467200-45487800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:45474000-45489000	Weak transcription	Primary T cells from cord blood	blood
6	chr6:45475000-45486000	Strong transcription	HSMM	muscle
7	chr6:45479000-45500000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr6:45480200-45488400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:45481000-45500200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:45481200-45487800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:45481400-45487000	Weak transcription	HSMMtube	muscle
12	chr6:45481400-45488200	Weak transcription	Fetal Lung	lung
13	chr6:45481400-45488600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr6:45481400-45500200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:45481400-45514600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:45482000-45488400	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr6:45482000-45490800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:45482000-45500000	Weak transcription	NHDF-Ad	bronchial
19	chr6:45482200-45488600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr6:45482400-45494600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr6:45482600-45487600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:45482600-45487600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:45482600-45487800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:45482600-45488000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:45482600-45488200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:45482600-45488200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:45482600-45489800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:45482600-45490200	Weak transcription	Dnd41	blood
29	chr6:45482600-45490400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:45482600-45490400	Weak transcription	NHLF	lung
31	chr6:45482600-45500200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:45482600-45503600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr6:45482800-45486000	Weak transcription	Fetal Thymus	thymus
34	chr6:45482800-45488000	Weak transcription	Stomach Mucosa	stomach
35	chr6:45482800-45514800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr6:45483000-45486000	Weak transcription	Osteobl	bone
37	chr6:45483000-45488600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr6:45483000-45490400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr6:45483400-45487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:45483600-45487800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr6:45483800-45487800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:45483800-45488000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr6:45484000-45488000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:45484200-45488000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:45484200-45488200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr6:45484400-45509400	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr6:45484400-45514600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr6:45484600-45486200	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr6:45484800-45486200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr6:45484800-45487800	Weak transcription	NH-A	brain

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