Variant report

Variant	nsv1049695
Chromosome Location	chr10:26870254-26914881
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	chr10:26895385-26895597	K562	blood:	n/a	n/a
2	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
4	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
5	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
6	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
7	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
8	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
9	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
10	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
11	CEBPB	chr10:26874087-26874199	A549	lung:	n/a	n/a
12	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr10:26883116-26883294	GM12878	blood:	n/a	n/a
14	CTCF	chr10:26896140-26896290	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr10:26899194-26899277	LNCaP	prostate:	n/a	n/a
16	CTCF	chr10:26895381-26895577	A549	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
17	CTCF	chr10:26895320-26895470	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:26895462-26895552	MCF-7	breast:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
19	CTCF	chr10:26895400-26895550	GM12865	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
20	CTCF	chr10:26895060-26895210	WI-38	lung:	n/a	n/a
21	CTCF	chr10:26875112-26875193	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:26895340-26895490	MCF-7	breast:	n/a	n/a
23	CTCF	chr10:26895400-26895550	HPF	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
24	CTCF	chr10:26895280-26895430	NHLF	lung:	n/a	n/a
25	CTCF	chr10:26895376-26895626	LNCaP	prostate:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
26	CTCF	chr10:26896040-26896190	GM12866	blood:	n/a	chr10:26896061-26896069
27	CTCF	chr10:26895400-26895550	HUVEC	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
28	CTCF	chr10:26895342-26895610	Lung_OC	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
29	CTCF	chr10:26895540-26895690	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr10:26895340-26895490	GM12871	blood:	n/a	n/a
31	CTCF	chr10:26875092-26875208	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:26894700-26894850	AG09319	gingival:	n/a	n/a
33	CTCF	chr10:26895340-26895490	GM12868	blood:	n/a	n/a
34	CTCF	chr10:26895280-26895430	HAc	cerebellar:	n/a	n/a
35	CTCF	chr10:26875117-26875119	GM19238	blood:	n/a	n/a
36	CTCF	chr10:26875099-26875292	K562	blood:	n/a	n/a
37	CTCF	chr10:26895420-26895570	HCPEpiC	choroid plexus:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
38	CTCF	chr10:26895340-26895490	GM12865	blood:	n/a	n/a
39	CTCF	chr10:26895600-26895750	HAc	cerebellar:	n/a	n/a
40	CTCF	chr10:26895280-26895430	A549	lung:	n/a	n/a
41	CTCF	chr10:26895540-26895690	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr10:26875090-26875309	GM12878	blood:	n/a	n/a
43	CTCF	chr10:26892341-26892412	NHEK	skin:	n/a	n/a
44	CTCF	chr10:26895540-26895690	NHEK	skin:	n/a	n/a
45	CTCF	chr10:26895480-26895630	GM12873	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
46	CTCF	chr10:26895353-26895644	Gliobla	brain:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
47	CTCF	chr10:26875091-26875200	MCF-7	breast:	n/a	n/a
48	CTCF	chr10:26895420-26895570	GM12864	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
49	CTCF	chr10:26895560-26895710	HCM	heart:	n/a	n/a
50	CTCF	chr10:26895540-26895690	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26878632-26878682	GM19239	blood:	n/a
2	chr10:26911186-26911236	SAEC	small airway:	n/a
3	chr10:26877803-26877853	HAEpiC	amniotic membrane:	n/a
4	chr10:26883165-26883215	K562	blood:	n/a
5	chr10:26911451-26911501	GM12891	blood:	n/a
6	chr10:26878632-26878682	ovcar-3	ovarian:	n/a
7	chr10:26877515-26877565	NB4	blood:	n/a
8	chr10:26877515-26877565	AG10803	skin:	n/a
9	chr10:26883165-26883215	Caco-2	colon:	n/a
10	chr10:26883013-26883063	NT2-D1	testis:	n/a
11	chr10:26877716-26877766	HAEpiC	amniotic membrane:	n/a
12	chr10:26883079-26883129	Jurkat	blood:	n/a
13	chr10:26911186-26911236	HMEC	breast:	n/a
14	chr10:26878627-26878677	GM19239	blood:	n/a
15	chr10:26877515-26877565	HAEpiC	amniotic membrane:	n/a
16	chr10:26911186-26911236	ECC-1	luminal epithelium:	n/a
17	chr10:26877803-26877853	ovcar-3	ovarian:	n/a
18	chr10:26881860-26881910	Hela-S3	cervix:	n/a
19	chr10:26877803-26877853	CMK	blood:	n/a
20	chr10:26877716-26877766	GM19239	blood:	n/a
21	chr10:26877515-26877565	AG04450	lung:	fetal
22	chr10:26878627-26878677	HRE	kidney:	n/a
23	chr10:26911451-26911501	HCPEpiC	choroid plexus:	n/a
24	chr10:26911451-26911501	HRCEpiC	kidney:	n/a
25	chr10:26881860-26881910	HCF	heart:	n/a
26	chr10:26877515-26877565	BE2_C	brain:	n/a
27	chr10:26877803-26877853	H1-hESC	embryonic stem cell:	embryo
28	chr10:26883079-26883129	MCF10A-Er-Src	breast:	n/a
29	chr10:26877803-26877853	IMR90	lung:	fetal
30	chr10:26877716-26877766	GM12891	blood:	n/a
31	chr10:26883165-26883215	SKMC	muscle:	n/a
32	chr10:26883013-26883063	AG04449	skin:	fetal
33	chr10:26878629-26878679	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:26883165-26883215	U87	brain:	n/a
35	chr10:26883013-26883063	SKMC	muscle:	n/a
36	chr10:26911451-26911501	ProgFib	skin:	n/a
37	chr10:26883165-26883215	NH-A	brain:	n/a
38	chr10:26878629-26878679	GM19239	blood:	n/a
39	chr10:26911451-26911501	AG04450	lung:	fetal
40	chr10:26883079-26883129	HEK293	kidney:	embryo
41	chr10:26883079-26883129	Hepatocyte	liver:	n/a
42	chr10:26883165-26883215	LNCaP	prostate:	n/a
43	chr10:26883013-26883063	ovcar-3	ovarian:	n/a
44	chr10:26883165-26883215	PrEC	prostate:	n/a
45	chr10:26878627-26878677	HIPEpiC	eye:	n/a
46	chr10:26877716-26877766	GM06990	blood:	n/a
47	chr10:26911451-26911501	GM12892	blood:	n/a
48	chr10:26878629-26878679	Hepatocyte	liver:	n/a
49	chr10:26877515-26877565	GM12891	blood:	n/a
50	chr10:26877803-26877853	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
2	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
3	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
4	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
5	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
6	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
2	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
3	lnc-PDSS1-1	chr10:26870673-26871754	NONHSAT011834
4	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
5	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
6	lnc-PDSS1-1	chr10:26878794-26879266	NR_026793
7	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
8	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
9	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
10	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
11	lnc-PDSS1-1	chr10:26879025-26879266	NONHSAT011840
12	lnc-APBB1IP-1	chr10:26876526-26877939	XLOC_008419
13	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
14	lnc-APBB1IP-1	chr10:26879064-26879266	XLOC_008419
15	lnc-PDSS1-1	chr10:26880239-26880342	NR_026793
16	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
17	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
18	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
19	lnc-PDSS1-1	chr10:26881779-26881895	NR_026793
20	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
21	lnc-APBB1IP-1	chr10:26881779-26882156	XLOC_008419
22	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
23	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
24	lnc-PDSS1-1	chr10:26882863-26883251	NR_026793

Variant related genes	Relation type
ENSG00000236894	TF binding region
LINC00264	TF binding region
ENSG00000236894	CpG island
LINC00264	CpG island
ZNF365	miRNA target sites
ZNF367	miRNA target sites

Extended variants
information (count: 2279 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2279 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs787006	chr10:26870254-26870255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146403720	chr10:26870272-26870273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377535025	chr10:26870286-26870287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192800800	chr10:26870303-26870304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184906300	chr10:26870325-26870326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540323442	chr10:26870358-26870359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562536651	chr10:26870364-26870365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531412746	chr10:26870387-26870388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs787005	chr10:26870397-26870398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs189028571	chr10:26870414-26870415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528682085	chr10:26870415-26870416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545554870	chr10:26870418-26870419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368275869	chr10:26870497-26870498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565062457	chr10:26870498-26870499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12242112	chr10:26870508-26870509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565454726	chr10:26870585-26870586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531092680	chr10:26870652-26870653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550587574	chr10:26870670-26870671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527591317	chr10:26870694-26870695	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs559598134	chr10:26870717-26870718	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs180944545	chr10:26870718-26870719	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs186357853	chr10:26870741-26870742	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs12773708	chr10:26870742-26870743	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs149627060	chr10:26870753-26870754	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs538474659	chr10:26870859-26870860	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs552334443	chr10:26870880-26870881	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs569205438	chr10:26870884-26870885	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs538135198	chr10:26870893-26870894	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs144333594	chr10:26870919-26870920	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs574495120	chr10:26870924-26870925	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs200808903	chr10:26870935-26870936	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs111894037	chr10:26870944-26870945	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs148432277	chr10:26870992-26870993	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs576838111	chr10:26871035-26871036	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs73594372	chr10:26871061-26871062	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs112663778	chr10:26871075-26871076	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs530005666	chr10:26871115-26871116	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs550135843	chr10:26871118-26871119	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs189590665	chr10:26871133-26871134	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs76487169	chr10:26871160-26871161	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs538745742	chr10:26871162-26871163	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs142539633	chr10:26871168-26871169	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs530866082	chr10:26871176-26871177	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs530036941	chr10:26871190-26871191	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546940795	chr10:26871195-26871196	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs560419609	chr10:26871213-26871214	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs57541993	chr10:26871235-26871236	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140265025	chr10:26871253-26871254	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs7091262	chr10:26871257-26871258	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565895287	chr10:26871273-26871274	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
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
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26857600-26880200	Weak transcription	Adipose Nuclei	Adipose
2	chr10:26858400-26879400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:26860800-26881200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr10:26861000-26874400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr10:26861200-26872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr10:26862400-26882400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr10:26863000-26879200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr10:26863200-26875200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr10:26864600-26875800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr10:26864600-26880400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr10:26864800-26875000	Weak transcription	Primary T cells from cord blood	blood
17	chr10:26864800-26875200	Weak transcription	Primary B cells from peripheral blood	blood
18	chr10:26864800-26881800	Weak transcription	Primary B cells from cord blood	blood
19	chr10:26864800-26882800	Weak transcription	Fetal Thymus	thymus
20	chr10:26865000-26874600	Weak transcription	Thymus	Thymus
21	chr10:26865000-26884600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr10:26867200-26884000	Weak transcription	Right Atrium	heart
23	chr10:26871600-26871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr10:26871600-26874800	Weak transcription	Spleen	Spleen
25	chr10:26871800-26874800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:26872400-26883000	Weak transcription	Gastric	stomach
27	chr10:26874600-26875600	Strong transcription	Thymus	Thymus
28	chr10:26874800-26875400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:26874800-26875400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:26874800-26875600	Strong transcription	Spleen	Spleen
31	chr10:26875000-26876000	Strong transcription	Primary T cells from cord blood	blood
32	chr10:26875200-26875600	Strong transcription	Primary B cells from peripheral blood	blood
33	chr10:26875200-26876200	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr10:26875600-26880800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr10:26875600-26881800	Weak transcription	Thymus	Thymus
36	chr10:26875600-26882800	Weak transcription	Spleen	Spleen
37	chr10:26875800-26876200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:26876000-26879200	Weak transcription	Primary T cells from cord blood	blood
39	chr10:26876200-26880200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr10:26876200-26882600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr10:26877600-26877800	Enhancers	Lung	lung
42	chr10:26878800-26884600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr10:26879000-26888400	Weak transcription	Liver	Liver
44	chr10:26879200-26880400	Strong transcription	Primary T cells from cord blood	blood
45	chr10:26879200-26881200	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr10:26879400-26881000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr10:26880200-26881000	Strong transcription	Adipose Nuclei	Adipose
48	chr10:26880200-26883400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr10:26880400-26881000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr10:26880400-26887400	Weak transcription	Primary T cells from cord blood	blood

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