Variant report

Variant	esv1797410
Chromosome Location	chr10:98983785-99041740
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	ARID3A	chr10:99038222-99039608	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:99038171-99038699	K562	blood:	n/a	n/a
3	ARID3A	chr10:98994217-98994515	HepG2	liver:	n/a	n/a
4	ATF3	chr10:99039246-99039441	K562	blood:	n/a	n/a
5	ATF3	chr10:99039088-99039522	K562	blood:	n/a	n/a
6	BACH1	chr10:99023131-99023176	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:99039478-99039637	K562	blood:	n/a	n/a
8	BATF	chr10:98990092-98990302	GM12878	blood:	n/a	n/a
9	BRCA1	chr10:99038906-99039407	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr10:99030500-99030894	K562	blood:	n/a	n/a
11	CEBPB	chr10:99039139-99039498	HepG2	liver:	n/a	chr10:99039305-99039316
12	CEBPB	chr10:98991022-98991230	K562	blood:	n/a	n/a
13	CEBPB	chr10:99039120-99039498	A549	lung:	n/a	chr10:99039305-99039316
14	CEBPB	chr10:99039052-99039536	A549	lung:	n/a	chr10:99039305-99039316
15	CEBPB	chr10:99039168-99039528	HepG2	liver:	n/a	chr10:99039305-99039316
16	CEBPB	chr10:99039120-99039504	HepG2	liver:	n/a	chr10:99039305-99039316
17	CEBPB	chr10:99038918-99039616	A549	lung:	n/a	chr10:99039305-99039316
18	CEBPB	chr10:99039116-99039500	K562	blood:	n/a	chr10:99039305-99039316
19	CEBPB	chr10:99039156-99039429	ECC-1	luminal epithelium:	n/a	chr10:99039305-99039316
20	CEBPB	chr10:99039117-99039430	K562	blood:	n/a	chr10:99039305-99039316
21	CEBPB	chr10:99039201-99039446	K562	blood:	n/a	chr10:99039305-99039316
22	CEBPB	chr10:99039123-99039497	IMR90	lung:	n/a	chr10:99039305-99039316
23	CEBPB	chr10:99039133-99039448	H1-hESC	embryonic stem cell:	n/a	chr10:99039305-99039316
24	CEBPB	chr10:99038261-99038602	K562	blood:	n/a	n/a
25	CEBPB	chr10:99026978-99027178	IMR90	lung:	n/a	chr10:99027053-99027064
26	CEBPB	chr10:99039163-99039409	HepG2	liver:	n/a	chr10:99039305-99039316
27	CEBPB	chr10:99027009-99027205	A549	lung:	n/a	chr10:99027053-99027064
28	CEBPB	chr10:99021342-99021463	K562	blood:	n/a	chr10:99021361-99021374 chr10:99021363-99021374
29	CEBPB	chr10:99026991-99027231	HepG2	liver:	n/a	chr10:99027053-99027064
30	CEBPB	chr10:99038323-99039525	Hela-S3	cervix:	n/a	chr10:99038662-99038673 chr10:99038662-99038673 chr10:99039305-99039316
31	CEBPB	chr10:99039132-99039525	MCF-7	breast:	n/a	chr10:99039305-99039316
32	CEBPD	chr10:99039199-99039407	HepG2	liver:	n/a	n/a
33	CEBPD	chr10:99039160-99039429	HepG2	liver:	n/a	n/a
34	CEBPD	chr10:99039110-99039504	K562	blood:	n/a	n/a
35	CEBPD	chr10:99039079-99039547	K562	blood:	n/a	n/a
36	CHD2	chr10:99039248-99039494	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr10:98995180-98995330	SAEC	small airway:	n/a	n/a
38	CTCF	chr10:98994640-98994790	HCFaa	heart:	n/a	n/a
39	CTCF	chr10:99038340-99038490	HCM	heart:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
40	CTCF	chr10:99038380-99038530	HRPEpiC	eye:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
41	CTCF	chr10:99038220-99038370	GM12870	blood:	n/a	n/a
42	CTCF	chr10:98994280-98994430	NHEK	skin:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
43	CTCF	chr10:99038380-99038530	HEEpiC	esophagus:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
44	CTCF	chr10:98994280-98994430	HMF	breast:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
45	CTCF	chr10:99038752-99038776	GM20000	blood:	n/a	n/a
46	CTCF	chr10:99003760-99003910	SAEC	small airway:	n/a	n/a
47	CTCF	chr10:99038360-99038510	HCPEpiC	choroid plexus:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
48	CTCF	chr10:99029620-99029770	AG09319	gingival:	n/a	n/a
49	CTCF	chr10:98994300-98994450	AG09319	gingival:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
50	CTCF	chr10:99038320-99038470	GM12801	blood:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442

No.	Distal block	Cell Line	Cell type
1	chr10:98982062..98983736-chr10:98992807..98994462,2	K562	blood:
2	chr10:99036915..99039794-chr10:99077195..99080138,2	MCF-7	breast:
3	chr10:98994406..98995974-chr10:98996173..98997856,2	K562	blood:
4	chr10:99029216..99031729-chr10:99037036..99038703,2	K562	blood:
5	chr10:98980598..98984541-chr10:98986940..98989319,3	K562	blood:
6	chr10:99038038..99038854-chr10:99093284..99094248,2	K562	blood:
7	chr10:99040683..99043669-chr10:99044105..99045670,2	MCF-7	breast:
8	chr10:99039203..99042240-chr10:99050005..99053012,5	K562	blood:
9	chr10:99037940..99038860-chr10:99115149..99115993,4	MCF-7	breast:
10	chr10:98976025..98978892-chr10:98984824..98987620,2	K562	blood:
11	chr10:99019069..99020733-chr10:99024295..99026088,2	K562	blood:
12	chr10:98980948..98983777-chr10:98984731..98986586,2	K562	blood:
13	chr10:99037600..99039792-chr10:99078754..99080411,2	K562	blood:
14	chr10:99038998..99042436-chr10:99050729..99053109,4	K562	blood:
15	chr10:99002077..99004456-chr10:99007278..99008816,2	K562	blood:
16	chr10:99002077..99004456-chr10:99007278..99008816,2	K562	blood:
17	chr10:98986271..98988962-chr10:98994711..98997131,2	K562	blood:
18	chr10:99028447..99031711-chr10:99092744..99094330,3	MCF-7	breast:
19	chr10:98994406..98995974-chr10:98996173..98997856,2	K562	blood:
20	chr10:99037958..99038944-chr10:99092338..99093941,8	MCF-7	breast:
21	chr10:98832712..98833218-chr10:98993851..98994375,2	MCF-7	breast:
22	chr10:99036931..99039171-chr10:99085750..99087329,2	K562	blood:
23	chr10:99002077..99004785-chr10:99007316..99010027,2	K562	blood:
24	chr10:99016160..99017870-chr10:99021990..99024984,2	MCF-7	breast:
25	chr10:99031855..99035094-chr10:99036519..99039061,3	K562	blood:
26	chr10:98986271..98988962-chr10:98994711..98997131,2	K562	blood:
27	chr10:98970315..98970824-chr10:98993860..98994647,2	MCF-7	breast:
28	chr10:99019069..99020733-chr10:99024295..99026088,2	K562	blood:
29	chr10:99014050..99016184-chr10:99078788..99081522,2	K562	blood:
30	chr10:98970361..98971335-chr10:98994318..98994830,2	K562	blood:
31	chr10:99002077..99004785-chr10:99007316..99010027,2	K562	blood:
32	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
33	chr10:98980598..98984541-chr10:98986940..98989319,3	K562	blood:
34	chr10:99030229..99033115-chr10:99036634..99039427,3	K562	blood:
35	chr10:98993826..98994564-chr10:99114704..99115929,4	MCF-7	breast:
36	chr10:99034381..99036020-chr10:99036062..99037985,2	K562	blood:
37	chr10:98876999..98877834-chr10:98994252..98994779,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRAT1-3	chr10:99037396-99037514	NONHSAT015852
2	lnc-FRAT1-3	chr10:99034769-99034864	NONHSAT015852
3	lnc-FRAT1-3	chr10:99037705-99037854	NONHSAT015852

Variant related genes	Relation type
ARHGAP19	TF binding region
ENSG00000231398	TF binding region
ENSG00000213390	chromatin interactions
ENSG00000165879	chromatin interactions
ENSG00000231398	chromatin interactions
ENSG00000225850	chromatin interactions
ENSG00000269891	chromatin interactions

Extended variants
information (count: 2207 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141408308	chr10:98983794-98983795	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374836395	chr10:98983860-98983861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375921518	chr10:98983862-98983863	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10748691	chr10:98983955-98983956	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs566255524	chr10:98983966-98983967	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564209506	chr10:98984011-98984012	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573894622	chr10:98984042-98984043	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201234130	chr10:98984056-98984057	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374327335	chr10:98984174-98984175	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570323060	chr10:98984267-98984268	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371019075	chr10:98984275-98984276	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12255418	chr10:98984297-98984298	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs12255419	chr10:98984312-98984313	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188626583	chr10:98984315-98984316	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553723917	chr10:98984316-98984317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571904538	chr10:98984327-98984328	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562788377	chr10:98984457-98984458	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs564047199	chr10:98984461-98984462	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs192528764	chr10:98984502-98984503	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs183558041	chr10:98984509-98984510	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs564855788	chr10:98984563-98984564	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs150859634	chr10:98984569-98984570	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs531862514	chr10:98984570-98984571	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs11189042	chr10:98984577-98984578	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529409961	chr10:98984585-98984586	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs547868206	chr10:98984630-98984631	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs187493036	chr10:98984652-98984653	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs533576887	chr10:98984671-98984672	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs534547701	chr10:98984685-98984686	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs139294445	chr10:98984689-98984690	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs568077808	chr10:98984691-98984692	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs192300539	chr10:98984718-98984719	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs701818	chr10:98984778-98984779	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184654460	chr10:98984824-98984825	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568037886	chr10:98984862-98984863	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145418411	chr10:98984902-98984903	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553833359	chr10:98985012-98985013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571765942	chr10:98985046-98985047	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12242381	chr10:98985056-98985057	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189928661	chr10:98985072-98985073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575968065	chr10:98985085-98985086	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192191353	chr10:98985104-98985105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1613575	chr10:98985144-98985145	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561989553	chr10:98985154-98985155	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184502071	chr10:98985193-98985194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147196520	chr10:98985229-98985230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12257293	chr10:98985239-98985240	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189133732	chr10:98985264-98985265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552031675	chr10:98985273-98985274	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563855889	chr10:98985360-98985361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1270 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98972400-98988400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:98973800-99019000	Weak transcription	HepG2	liver
3	chr10:98974000-98986200	Weak transcription	Pancreas	Pancrea
4	chr10:98976000-99011400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr10:98976400-98988200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr10:98976800-98988200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr10:98977200-99023800	Weak transcription	Colonic Mucosa	Colon
8	chr10:98977400-99027000	Weak transcription	Right Ventricle	heart
9	chr10:98977600-98984800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:98978200-98985000	Weak transcription	Adipose Nuclei	Adipose
11	chr10:98978200-98985600	Weak transcription	HMEC	breast
12	chr10:98978200-99003400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:98978200-99003600	Weak transcription	NHEK	skin
14	chr10:98978600-98983800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:98978600-98984000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr10:98978600-98984400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:98978600-98984400	Weak transcription	NHDF-Ad	bronchial
18	chr10:98978600-98985600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:98978600-98988800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr10:98978600-99019000	Weak transcription	HSMMtube	muscle
21	chr10:98978600-99030400	Weak transcription	NH-A	brain
22	chr10:98978600-99037400	Weak transcription	HSMM	muscle
23	chr10:98978600-99051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr10:98979000-98984200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:98979000-98984800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr10:98979000-98990400	Strong transcription	Fetal Thymus	thymus
27	chr10:98979000-99027400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr10:98979200-98984600	Weak transcription	HUVEC	blood vessel
29	chr10:98979200-98987200	Weak transcription	Fetal Intestine Large	intestine
30	chr10:98979400-98984800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:98979400-98989600	Weak transcription	NHLF	lung
32	chr10:98979400-99000600	Strong transcription	Dnd41	blood
33	chr10:98979600-98990000	Strong transcription	Thymus	Thymus
34	chr10:98979600-99003400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr10:98980000-98984400	Weak transcription	Gastric	stomach
36	chr10:98980200-98986200	Strong transcription	Fetal Intestine Small	intestine
37	chr10:98980200-98987000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr10:98980200-98989600	Strong transcription	Primary T cells from cord blood	blood
39	chr10:98980200-98992800	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr10:98980400-98988000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr10:98980600-98984000	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr10:98980600-98990400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr10:98980800-98987000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr10:98980800-98988800	Weak transcription	A549	lung
45	chr10:98981000-98987200	Strong transcription	Fetal Stomach	stomach
46	chr10:98981000-99018200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr10:98981200-98984400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr10:98981200-98984400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr10:98981400-98984200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr10:98981400-98989200	Strong transcription	Fetal Muscle Leg	muscle

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