Variant report

Variant	esv2759736
Chromosome Location	chr10:18835325-18906507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1055)
CpG islands
(count:366)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:18850803-18851483	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:18847006-18847183	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:18871855-18872156	K562	blood:	n/a	n/a
4	ARID3A	chr10:18904510-18904940	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:18854097-18854130	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:18843485-18843910	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:18872609-18872929	K562	blood:	n/a	n/a
8	ARID3A	chr10:18855015-18855499	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:18852867-18853155	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:18883708-18883996	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:18899277-18899936	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:18905265-18905558	HepG2	liver:	n/a	n/a
13	ATF1	chr10:18871829-18872244	K562	blood:	n/a	n/a
14	ATF3	chr10:18899316-18899918	A549	lung:	n/a	n/a
15	ATF3	chr10:18899422-18899773	K562	blood:	n/a	n/a
16	BCL3	chr10:18899399-18899889	A549	lung:	n/a	chr10:18899618-18899627 chr10:18899617-18899626
17	BCL3	chr10:18899259-18899915	A549	lung:	n/a	chr10:18899618-18899627 chr10:18899617-18899626
18	BHLHE40	chr10:18883841-18883953	K562	blood:	n/a	n/a
19	BHLHE40	chr10:18899416-18899774	HepG2	liver:	n/a	n/a
20	BRCA1	chr10:18860127-18860500	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr10:18860126-18860500	GM12878	blood:	n/a	n/a
22	BRCA1	chr10:18848238-18848611	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr10:18899413-18899828	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr10:18899306-18899911	HCT-116	colon:	n/a	n/a
25	CBX3	chr10:18866717-18867121	K562	blood:	n/a	n/a
26	CBX3	chr10:18866819-18867030	K562	blood:	n/a	n/a
27	CEBPB	chr10:18899142-18899339	K562	blood:	n/a	n/a
28	CEBPB	chr10:18899123-18899850	HepG2	liver:	n/a	n/a
29	CEBPB	chr10:18899390-18899875	MCF-7	breast:	n/a	n/a
30	CEBPB	chr10:18905309-18905644	A549	lung:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
31	CEBPB	chr10:18899357-18899980	HCT-116	colon:	n/a	n/a
32	CEBPB	chr10:18899449-18899705	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:18899297-18899950	A549	lung:	n/a	n/a
34	CEBPB	chr10:18905277-18905663	Hela-S3	cervix:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
35	CEBPB	chr10:18906025-18906328	K562	blood:	n/a	chr10:18906172-18906183
36	CEBPB	chr10:18904547-18904932	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:18855132-18855383	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr10:18897524-18897856	A549	lung:	n/a	n/a
39	CEBPB	chr10:18906026-18906333	A549	lung:	n/a	chr10:18906172-18906183
40	CEBPB	chr10:18899369-18899850	A549	lung:	n/a	n/a
41	CEBPB	chr10:18899351-18899802	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:18906018-18906303	MCF-7	breast:	n/a	chr10:18906172-18906183
43	CEBPB	chr10:18899386-18899890	MCF-7	breast:	n/a	n/a
44	CEBPB	chr10:18872595-18872894	K562	blood:	n/a	n/a
45	CEBPB	chr10:18905221-18905642	MCF-7	breast:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
46	CEBPB	chr10:18896414-18896838	A549	lung:	n/a	n/a
47	CEBPB	chr10:18905239-18905623	HepG2	liver:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
48	CEBPB	chr10:18899349-18899886	A549	lung:	n/a	n/a
49	CEBPB	chr10:18905280-18905585	MCF-7	breast:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
50	CEBPB	chr10:18890961-18891104	IMR90	lung:	n/a	chr10:18891048-18891059

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:18875548-18875598	HCF	heart:	n/a
2	chr10:18877005-18877055	HRE	kidney:	n/a
3	chr10:18898790-18898840	HCF	heart:	n/a
4	chr10:18875548-18875598	SK-N-MC	brain:	n/a
5	chr10:18898790-18898840	AG09319	gingival:	n/a
6	chr10:18875548-18875598	AG10803	skin:	n/a
7	chr10:18877005-18877055	MCF10A-Er-Src	breast:	n/a
8	chr10:18877005-18877055	HEK293	kidney:	embryo
9	chr10:18895474-18895524	H1-hESC	embryonic stem cell:	embryo
10	chr10:18875548-18875598	NHBE	bronchial:	n/a
11	chr10:18875548-18875598	U87	brain:	n/a
12	chr10:18875473-18875523	ECC-1	luminal epithelium:	n/a
13	chr10:18875548-18875598	LNCaP	prostate:	n/a
14	chr10:18895474-18895524	AoSMC	blood vessel:	n/a
15	chr10:18875381-18875431	NB4	blood:	n/a
16	chr10:18875548-18875598	NH-A	brain:	n/a
17	chr10:18877005-18877055	AG09319	gingival:	n/a
18	chr10:18875381-18875431	NHBE	bronchial:	n/a
19	chr10:18875381-18875431	PFSK-1	brain:	n/a
20	chr10:18898790-18898840	HRCEpiC	kidney:	n/a
21	chr10:18875548-18875598	Hela-S3	cervix:	n/a
22	chr10:18875548-18875598	GM12892	blood:	n/a
23	chr10:18895474-18895524	BJ	skin:	n/a
24	chr10:18875548-18875598	HAEpiC	amniotic membrane:	n/a
25	chr10:18875473-18875523	AG04449	skin:	fetal
26	chr10:18875473-18875523	HCF	heart:	n/a
27	chr10:18877005-18877055	NB4	blood:	n/a
28	chr10:18875381-18875431	SAEC	small airway:	n/a
29	chr10:18875381-18875431	GM12892	blood:	n/a
30	chr10:18898790-18898840	K562	blood:	n/a
31	chr10:18875473-18875523	Hepatocyte	liver:	n/a
32	chr10:18875548-18875598	SK-N-SH_RA	brain:	n/a
33	chr10:18875548-18875598	HRCEpiC	kidney:	n/a
34	chr10:18875381-18875431	SK-N-SH	brain:	n/a
35	chr10:18875473-18875523	LNCaP	prostate:	n/a
36	chr10:18898790-18898840	HCM	heart:	n/a
37	chr10:18895474-18895524	HepG2	liver:	n/a
38	chr10:18875548-18875598	HMEC	breast:	n/a
39	chr10:18877005-18877055	BJ	skin:	n/a
40	chr10:18898790-18898840	HRPEpiC	eye:	n/a
41	chr10:18875548-18875598	IMR90	lung:	fetal
42	chr10:18895474-18895524	HUVEC	blood vessel:	n/a
43	chr10:18875381-18875431	CMK	blood:	n/a
44	chr10:18898790-18898840	AG09309	skin:	n/a
45	chr10:18898790-18898840	GM19239	blood:	n/a
46	chr10:18875381-18875431	PrEC	prostate:	n/a
47	chr10:18895474-18895524	PrEC	prostate:	n/a
48	chr10:18895474-18895524	Hela-S3	cervix:	n/a
49	chr10:18875548-18875598	NHDF-neo	bronchial:	n/a
50	chr10:18875381-18875431	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:18872028..18874928-chr10:18946049..18948722,4	K562	blood:
2	chr10:18896603..18898658-chr10:18901969..18903863,2	K562	blood:
3	chr10:18900986..18902692-chr10:18906814..18908491,2	MCF-7	breast:
4	chr10:18871041..18872755-chr10:18938799..18941399,2	K562	blood:
5	chr1:1025004..1026004-chr10:18883636..18884321,2	MCF-7	breast:
6	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:
7	chr10:18892806..18896035-chr10:18901171..18903670,3	K562	blood:
8	chr10:18897158..18899309-chr10:18901969..18904753,2	K562	blood:
9	chr10:18883515..18884111-chr10:18904979..18905887,2	MCF-7	breast:
10	chr10:18881247..18884193-chr10:18945949..18949026,3	K562	blood:
11	chr10:18881247..18884169-chr10:18946476..18949026,2	K562	blood:
12	chr10:18902407..18904405-chr10:18907032..18908667,2	K562	blood:
13	chr10:18901454..18904568-chr10:18946720..18950711,3	K562	blood:
14	chr10:18897158..18899309-chr10:18901969..18904753,2	K562	blood:
15	chr10:18891764..18894660-chr10:18898788..18901660,3	K562	blood:
16	chr10:18893160..18894729-chr10:18899323..18901039,2	K562	blood:
17	chr10:18883515..18884111-chr10:18904979..18905887,2	MCF-7	breast:
18	chr10:18892806..18896035-chr10:18901171..18903670,3	K562	blood:
19	chr10:18832497..18833999-chr10:18887489..18889225,2	K562	blood:
20	chr10:18904719..18906384-chr10:18907466..18910292,2	K562	blood:
21	chr10:18896603..18898658-chr10:18901969..18903863,2	K562	blood:
22	chr10:18891764..18894660-chr10:18898788..18901660,3	K562	blood:
23	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:
24	chr10:18893160..18894729-chr10:18899323..18901039,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000240291	TF binding region
NSUN6	TF binding region
ENSG00000240291	CpG island
NSUN6	CpG island
ENSG00000152487	chromatin interactions
ENSG00000165997	chromatin interactions
ENSG00000240291	chromatin interactions
ENSG00000241058	chromatin interactions

Extended variants
information (count: 3808 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:3808 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10764584	chr10:18835325-18835326	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10828879	chr10:18835354-18835355	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs114336917	chr10:18835358-18835359	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191436206	chr10:18835423-18835424	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs528460141	chr10:18835453-18835454	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546706294	chr10:18835487-18835488	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs139562258	chr10:18835495-18835496	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538791277	chr10:18835564-18835565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550761275	chr10:18835572-18835573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569059494	chr10:18835577-18835578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536456702	chr10:18835617-18835618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555207445	chr10:18835626-18835627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577944869	chr10:18835652-18835653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547777603	chr10:18835668-18835669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533760228	chr10:18835674-18835675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144274198	chr10:18835676-18835677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577001412	chr10:18835726-18835727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367640135	chr10:18835776-18835777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562581219	chr10:18835779-18835780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146584917	chr10:18835780-18835781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112512935	chr10:18835782-18835783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574118380	chr10:18835792-18835793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560375168	chr10:18835813-18835814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544889492	chr10:18835815-18835816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369227475	chr10:18835816-18835817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370859419	chr10:18835835-18835836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527625910	chr10:18835854-18835855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544412992	chr10:18835861-18835862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375228209	chr10:18835878-18835879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560249098	chr10:18835882-18835883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183616339	chr10:18835891-18835892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532376579	chr10:18835900-18835901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550618180	chr10:18835919-18835920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187771347	chr10:18835927-18835928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192339398	chr10:18835928-18835929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567756470	chr10:18835935-18835936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12258119	chr10:18835936-18835937	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs141334371	chr10:18835958-18835959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185232525	chr10:18835979-18835980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570414534	chr10:18836031-18836032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537857363	chr10:18836032-18836033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375725289	chr10:18836070-18836071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556265594	chr10:18836072-18836073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574613950	chr10:18836098-18836099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149828822	chr10:18836150-18836151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553726310	chr10:18836162-18836163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145844135	chr10:18836185-18836186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545735260	chr10:18836202-18836203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564047178	chr10:18836213-18836214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532336189	chr10:18836228-18836229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18815200-18843600	Weak transcription	A549	lung
2	chr10:18816400-18841800	Strong transcription	Liver	Liver
3	chr10:18820800-18841600	Weak transcription	Hela-S3	cervix
4	chr10:18822000-18840400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr10:18822000-18848000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr10:18822800-18841800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:18823600-18836600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:18824200-18846200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr10:18824200-18850600	Weak transcription	NHLF	lung
10	chr10:18825000-18835800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:18825600-18841800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr10:18827000-18835800	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr10:18827200-18842000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr10:18827200-18845200	Weak transcription	NHEK	skin
15	chr10:18827400-18841600	Weak transcription	HMEC	breast
16	chr10:18827600-18839400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:18828600-18837800	Weak transcription	Psoas Muscle	Psoas
18	chr10:18828600-18838800	Weak transcription	Colonic Mucosa	Colon
19	chr10:18828600-18841600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr10:18828600-18841600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr10:18828600-18841800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:18828600-18841800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:18828600-18841800	Weak transcription	Pancreas	Pancrea
24	chr10:18828600-18843000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr10:18828600-18843400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr10:18828600-18844400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr10:18828600-18845400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:18828800-18846000	Weak transcription	Spleen	Spleen
29	chr10:18829000-18840400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr10:18829000-18841800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr10:18829200-18851200	Weak transcription	Esophagus	oesophagus
32	chr10:18829800-18837400	Weak transcription	GM12878-XiMat	blood
33	chr10:18829800-18838000	Weak transcription	Right Ventricle	heart
34	chr10:18829800-18844000	Weak transcription	Brain Angular Gyrus	brain
35	chr10:18830000-18842000	Weak transcription	Fetal Brain Female	brain
36	chr10:18830000-18842400	Weak transcription	Brain Germinal Matrix	brain
37	chr10:18830200-18841400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr10:18830200-18841800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr10:18830200-18841800	Weak transcription	Aorta	Aorta
40	chr10:18830200-18851000	Weak transcription	Thymus	Thymus
41	chr10:18830400-18837000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:18830400-18837800	Weak transcription	Primary B cells from cord blood	blood
43	chr10:18830400-18838400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr10:18830400-18839200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr10:18830400-18840000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:18830400-18840200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr10:18830400-18840400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr10:18830400-18840400	Weak transcription	Brain Anterior Caudate	brain
49	chr10:18830400-18840400	Weak transcription	HSMMtube	muscle
50	chr10:18830400-18841600	Weak transcription	H9 Cell Line	embryonic stem cell

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