Variant report

Variant	nsv550231
Chromosome Location	chr10:26866420-26908475
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	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
3	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
4	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
5	CEBPB	chr10:26874087-26874199	A549	lung:	n/a	n/a
6	CHD2	chr10:26883116-26883294	GM12878	blood:	n/a	n/a
7	CTCF	chr10:26895359-26895608	Pancreas_OC	pancreas:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
8	CTCF	chr10:26875090-26875309	GM12878	blood:	n/a	n/a
9	CTCF	chr10:26895380-26895530	K562	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
10	CTCF	chr10:26895300-26895450	RPTEC	kidney:	n/a	n/a
11	CTCF	chr10:26895260-26895410	GM12870	blood:	n/a	n/a
12	CTCF	chr10:26895462-26895552	MCF-7	breast:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
13	CTCF	chr10:26895368-26895635	MCF-7	breast:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
14	CTCF	chr10:26895340-26895490	HVMF	connective:	n/a	n/a
15	CTCF	chr10:26895300-26895450	HCM	heart:	n/a	n/a
16	CTCF	chr10:26895040-26895190	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr10:26895560-26895710	HMEC	breast:	n/a	n/a
18	CTCF	chr10:26895380-26895612	Kidney_OC	kidney:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
19	CTCF	chr10:26875090-26875221	GM19240	blood:	n/a	n/a
20	CTCF	chr10:26892326-26892398	Gliobla	brain:	n/a	n/a
21	CTCF	chr10:26895420-26895570	Caco-2	colon:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
22	CTCF	chr10:26895340-26895630	WI-38	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
23	CTCF	chr10:26895351-26895642	MCF-7	breast:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
24	CTCF	chr10:26875099-26875292	K562	blood:	n/a	n/a
25	CTCF	chr10:26895332-26895680	A549	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
26	CTCF	chr10:26903851-26903881	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr10:26895417-26895608	A549	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
28	CTCF	chr10:26895540-26895690	HEK293	kidney:	n/a	n/a
29	CTCF	chr10:26895320-26895470	HCM	heart:	n/a	n/a
30	CTCF	chr10:26908392-26908453	GM20000	blood:	n/a	n/a
31	CTCF	chr10:26894340-26894490	BJ	skin:	n/a	n/a
32	CTCF	chr10:26895540-26895690	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr10:26895540-26895690	GM12869	blood:	n/a	n/a
34	CTCF	chr10:26895560-26895710	HCT-116	colon:	n/a	n/a
35	CTCF	chr10:26895400-26895550	HMEC	breast:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
36	CTCF	chr10:26895280-26895430	A549	lung:	n/a	n/a
37	CTCF	chr10:26895355-26895625	Hela-S3	cervix:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
38	CTCF	chr10:26895320-26895470	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr10:26895400-26895550	GM12865	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
40	CTCF	chr10:26895540-26895690	RPTEC	kidney:	n/a	n/a
41	CTCF	chr10:26895420-26895570	SK-N-SH_RA	brain:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
42	CTCF	chr10:26895320-26895470	HFF	foreskin:	n/a	n/a
43	CTCF	chr10:26875117-26875119	GM19238	blood:	n/a	n/a
44	CTCF	chr10:26882575-26882604	GM13976	blood:	n/a	n/a
45	CTCF	chr10:26895400-26895550	AG09309	skin:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
46	CTCF	chr10:26895400-26895550	HPAF	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
47	CTCF	chr10:26895320-26895470	BE2_C	brain:	n/a	n/a
48	CTCF	chr10:26895354-26895613	GM12878	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
49	CTCF	chr10:26895320-26895470	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr10:26895560-26895710	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26877716-26877766	A549	lung:	n/a
2	chr10:26877716-26877766	A549	lung:	n/a
3	chr10:26878629-26878679	Hela-S3	cervix:	n/a
4	chr10:26877716-26877766	AG09309	skin:	n/a
5	chr10:26877716-26877766	SK-N-SH	brain:	n/a
6	chr10:26877716-26877766	Caco-2	colon:	n/a
7	chr10:26878629-26878679	GM12892	blood:	n/a
8	chr10:26881860-26881910	ProgFib	skin:	n/a
9	chr10:26877716-26877766	GM06990	blood:	n/a
10	chr10:26877716-26877766	IMR90	lung:	fetal
11	chr10:26877716-26877766	ECC-1	luminal epithelium:	n/a
12	chr10:26877515-26877565	HRE	kidney:	n/a
13	chr10:26881860-26881910	SK-N-SH_RA	brain:	n/a
14	chr10:26881860-26881910	HRPEpiC	eye:	n/a
15	chr10:26878632-26878682	NB4	blood:	n/a
16	chr10:26877716-26877766	SK-N-SH_RA	brain:	n/a
17	chr10:26877515-26877565	IMR90	lung:	fetal
18	chr10:26881860-26881910	SK-N-MC	brain:	n/a
19	chr10:26877803-26877853	Hepatocyte	liver:	n/a
20	chr10:26877515-26877565	K562	blood:	n/a
21	chr10:26877515-26877565	MCF10A-Er-Src	breast:	n/a
22	chr10:26877803-26877853	SKMC	muscle:	n/a
23	chr10:26877515-26877565	LNCaP	prostate:	n/a
24	chr10:26878632-26878682	BE2_C	brain:	n/a
25	chr10:26883079-26883129	ECC-1	luminal epithelium:	n/a
26	chr10:26877515-26877565	NH-A	brain:	n/a
27	chr10:26877716-26877766	HEEpiC	esophagus:	n/a
28	chr10:26883165-26883215	CMK	blood:	n/a
29	chr10:26883013-26883063	Jurkat	blood:	n/a
30	chr10:26878629-26878679	MCF-7	breast:	n/a
31	chr10:26883165-26883215	HCM	heart:	n/a
32	chr10:26877803-26877853	NB4	blood:	n/a
33	chr10:26883165-26883215	Caco-2	colon:	n/a
34	chr10:26877716-26877766	AG09319	gingival:	n/a
35	chr10:26883013-26883063	AG04449	skin:	fetal
36	chr10:26877716-26877766	HNPCEpiC	eye:	n/a
37	chr10:26878629-26878679	HL-60	blood:	n/a
38	chr10:26878627-26878677	SK-N-SH	brain:	n/a
39	chr10:26883079-26883129	SK-N-MC	brain:	n/a
40	chr10:26877803-26877853	NHDF-neo	bronchial:	n/a
41	chr10:26878627-26878677	HCF	heart:	n/a
42	chr10:26878632-26878682	HAEpiC	amniotic membrane:	n/a
43	chr10:26877515-26877565	HNPCEpiC	eye:	n/a
44	chr10:26877803-26877853	NH-A	brain:	n/a
45	chr10:26883165-26883215	HPAEpiC	pulmonary alveolar:	n/a
46	chr10:26883079-26883129	PrEC	prostate:	n/a
47	chr10:26878629-26878679	SK-N-MC	brain:	n/a
48	chr10:26877803-26877853	BE2_C	brain:	n/a
49	chr10:26878629-26878679	Caco-2	colon:	n/a
50	chr10:26883165-26883215	K562	blood:	n/a

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

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

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

Extended variants
information (count: 2068 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4747570	chr10:26866420-26866421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542319077	chr10:26866502-26866503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531467803	chr10:26866512-26866513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547585328	chr10:26866548-26866549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534933059	chr10:26866573-26866574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4747571	chr10:26866579-26866580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549561534	chr10:26866592-26866593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569626926	chr10:26866607-26866608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115265183	chr10:26866613-26866614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs180842992	chr10:26866619-26866620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12256600	chr10:26866634-26866635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs550415316	chr10:26866665-26866666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386742144	chr10:26866666-26866667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534141469	chr10:26866667-26866668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561369747	chr10:26866679-26866680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554327882	chr10:26866687-26866688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577495372	chr10:26866707-26866708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546473438	chr10:26866708-26866709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556323379	chr10:26866728-26866729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186127321	chr10:26866805-26866806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542197357	chr10:26866816-26866817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562183363	chr10:26866838-26866839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375035157	chr10:26866841-26866842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527749558	chr10:26866958-26866959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371425143	chr10:26866990-26866991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146370914	chr10:26867002-26867003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564281466	chr10:26867011-26867012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192285907	chr10:26867021-26867022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181780104	chr10:26867031-26867032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569805489	chr10:26867039-26867040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79648699	chr10:26867041-26867042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547694078	chr10:26867080-26867081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11814809	chr10:26867093-26867094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534391722	chr10:26867149-26867150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554118007	chr10:26867157-26867158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571015677	chr10:26867161-26867162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539645069	chr10:26867172-26867173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556817797	chr10:26867266-26867267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576780413	chr10:26867285-26867286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35062921	chr10:26867294-26867295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542258117	chr10:26867315-26867316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114248541	chr10:26867331-26867332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186478476	chr10:26867366-26867367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541509049	chr10:26867369-26867370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564387032	chr10:26867370-26867371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533156135	chr10:26867385-26867386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543225316	chr10:26867404-26867405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190519864	chr10:26867450-26867451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555029249	chr10:26867470-26867471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs36094822	chr10:26867516-26867517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

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

Chromatin state (count:122 , 50 per page) page: 1 2 3

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	chr10:26863000-26867000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:26863000-26879200	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr10:26863200-26875200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr10:26864600-26875800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr10:26864600-26880400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr10:26864800-26875000	Weak transcription	Primary T cells from cord blood	blood
18	chr10:26864800-26875200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr10:26864800-26881800	Weak transcription	Primary B cells from cord blood	blood
20	chr10:26864800-26882800	Weak transcription	Fetal Thymus	thymus
21	chr10:26865000-26874600	Weak transcription	Thymus	Thymus
22	chr10:26865000-26884600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr10:26867000-26867600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr10:26867200-26884000	Weak transcription	Right Atrium	heart
25	chr10:26871600-26871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:26871600-26874800	Weak transcription	Spleen	Spleen
27	chr10:26871800-26874800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:26872400-26883000	Weak transcription	Gastric	stomach
29	chr10:26874600-26875600	Strong transcription	Thymus	Thymus
30	chr10:26874800-26875400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr10:26874800-26875400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:26874800-26875600	Strong transcription	Spleen	Spleen
33	chr10:26875000-26876000	Strong transcription	Primary T cells from cord blood	blood
34	chr10:26875200-26875600	Strong transcription	Primary B cells from peripheral blood	blood
35	chr10:26875200-26876200	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr10:26875600-26880800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr10:26875600-26881800	Weak transcription	Thymus	Thymus
38	chr10:26875600-26882800	Weak transcription	Spleen	Spleen
39	chr10:26875800-26876200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr10:26876000-26879200	Weak transcription	Primary T cells from cord blood	blood
41	chr10:26876200-26880200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr10:26876200-26882600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr10:26877600-26877800	Enhancers	Lung	lung
44	chr10:26878800-26884600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr10:26879000-26888400	Weak transcription	Liver	Liver
46	chr10:26879200-26880400	Strong transcription	Primary T cells from cord blood	blood
47	chr10:26879200-26881200	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr10:26879400-26881000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr10:26880200-26881000	Strong transcription	Adipose Nuclei	Adipose
50	chr10:26880200-26883400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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