Variant report

Variant	esv3409599
Chromosome Location	chr10:26860997-26947298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:952)
CpG islands
(count:1528)
Chromatin interactive
region (count:9)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	ATF2	chr10:26863707-26864194	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26863637-26864211	GM12878	blood:	n/a	n/a
4	ATF2	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
5	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
6	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
7	ATF3	chr10:26863854-26863990	GM12878	blood:	n/a	n/a
8	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
10	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
11	BATF	chr10:26862524-26862900	GM12878	blood:	n/a	n/a
12	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
13	BATF	chr10:26863697-26864149	GM12878	blood:	n/a	n/a
14	BATF	chr10:26863751-26864136	GM12878	blood:	n/a	n/a
15	BATF	chr10:26862573-26862909	GM12878	blood:	n/a	n/a
16	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
17	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:26863793-26864021	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:26862584-26862977	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
21	BCL11A	chr10:26863648-26864087	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:26863786-26864104	GM12878	blood:	n/a	n/a
23	BCLAF1	chr10:26863717-26864158	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:26862634-26862906	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:26863731-26864167	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
28	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
29	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
30	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
32	CEBPB	chr10:26860662-26861015	A549	lung:	n/a	chr10:26860826-26860837
33	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
34	CEBPB	chr10:26860646-26861004	MCF-7	breast:	n/a	chr10:26860826-26860837
35	CEBPB	chr10:26860649-26861015	IMR90	lung:	n/a	chr10:26860826-26860837
36	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
38	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
39	CEBPB	chr10:26874087-26874199	A549	lung:	n/a	n/a
40	CEBPB	chr10:26860641-26861006	HepG2	liver:	n/a	chr10:26860826-26860837
41	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
42	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
43	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
44	CHD1	chr10:26862678-26862878	GM12878	blood:	n/a	n/a
45	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr10:26862700-26862938	GM12878	blood:	n/a	n/a
47	CHD2	chr10:26862199-26862219	GM12878	blood:	n/a	n/a
48	CHD2	chr10:26883116-26883294	GM12878	blood:	n/a	n/a
49	CREB1	chr10:26863824-26864151	GM12878	blood:	n/a	n/a
50	CTCF	chr10:26862660-26862810	AG10803	skin:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26881860-26881910	CMK	blood:	n/a
2	chr10:26932057-26932107	HEK293	kidney:	embryo
3	chr10:26883013-26883063	PFSK-1	brain:	n/a
4	chr10:26881860-26881910	CMK	blood:	n/a
5	chr10:26932057-26932107	HEK293	kidney:	embryo
6	chr10:26883013-26883063	PFSK-1	brain:	n/a
7	chr10:26883013-26883063	HRCEpiC	kidney:	n/a
8	chr10:26931991-26932041	GM12891	blood:	n/a
9	chr10:26931731-26931781	SK-N-SH_RA	brain:	n/a
10	chr10:26911186-26911236	SK-N-SH_RA	brain:	n/a
11	chr10:26881860-26881910	HL-60	blood:	n/a
12	chr10:26878629-26878679	HPAEpiC	pulmonary alveolar:	n/a
13	chr10:26881860-26881910	K562	blood:	n/a
14	chr10:26942165-26942215	AoSMC	blood vessel:	n/a
15	chr10:26911186-26911236	HUVEC	blood vessel:	n/a
16	chr10:26877515-26877565	HUVEC	blood vessel:	n/a
17	chr10:26931986-26932036	PFSK-1	brain:	n/a
18	chr10:26877716-26877766	MCF10A-Er-Src	breast:	n/a
19	chr10:26878632-26878682	HNPCEpiC	eye:	n/a
20	chr10:26932057-26932107	HepG2	liver:	n/a
21	chr10:26883165-26883215	HCM	heart:	n/a
22	chr10:26911186-26911236	A549	lung:	n/a
23	chr10:26877716-26877766	ovcar-3	ovarian:	n/a
24	chr10:26931912-26931962	RPTEC	kidney:	n/a
25	chr10:26931991-26932041	PrEC	prostate:	n/a
26	chr10:26877803-26877853	HL-60	blood:	n/a
27	chr10:26931926-26931976	HCT-116	colon:	n/a
28	chr10:26931991-26932041	BJ	skin:	n/a
29	chr10:26942165-26942215	AG04450	lung:	fetal
30	chr10:26942225-26942275	HNPCEpiC	eye:	n/a
31	chr10:26878632-26878682	HRCEpiC	kidney:	n/a
32	chr10:26878629-26878679	ECC-1	luminal epithelium:	n/a
33	chr10:26931986-26932036	SAEC	small airway:	n/a
34	chr10:26931969-26932019	SK-N-SH_RA	brain:	n/a
35	chr10:26931794-26931844	HCM	heart:	n/a
36	chr10:26877515-26877565	GM06990	blood:	n/a
37	chr10:26911186-26911236	PrEC	prostate:	n/a
38	chr10:26931978-26932028	ProgFib	skin:	n/a
39	chr10:26931991-26932041	T-47D	breast:	n/a
40	chr10:26931991-26932041	CMK	blood:	n/a
41	chr10:26931794-26931844	Hepatocyte	liver:	n/a
42	chr10:26930863-26930913	SK-N-SH	brain:	n/a
43	chr10:26931986-26932036	NB4	blood:	n/a
44	chr10:26883165-26883215	LNCaP	prostate:	n/a
45	chr10:26877515-26877565	T-47D	breast:	n/a
46	chr10:26877515-26877565	NB4	blood:	n/a
47	chr10:26883165-26883215	HRCEpiC	kidney:	n/a
48	chr10:26931986-26932036	Caco-2	colon:	n/a
49	chr10:26877803-26877853	GM12891	blood:	n/a
50	chr10:26883079-26883129	HIPEpiC	eye:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
2	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
3	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
4	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
5	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
6	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
7	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
8	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
9	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
2	lnc-PDSS1-1	chr10:26879025-26879266	NONHSAT011840
3	lnc-APBB1IP-1	chr10:26879064-26879266	XLOC_008419
4	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
5	lnc-PDSS1-1	chr10:26881779-26881895	NR_026793
6	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
7	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
8	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
9	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
10	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
11	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
12	lnc-PDSS1-1	chr10:26878794-26879266	NR_026793
13	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
14	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
15	lnc-PDSS1-1	chr10:26880239-26880342	NR_026793
16	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
17	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
18	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
19	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
20	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
21	lnc-APBB1IP-1	chr10:26881779-26882156	XLOC_008419
22	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
23	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
24	lnc-APBB1IP-1	chr10:26876526-26877939	XLOC_008419
25	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
26	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
27	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
28	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
29	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
30	lnc-PDSS1-1	chr10:26870673-26871754	NONHSAT011834
31	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
32	lnc-PDSS1-1	chr10:26882863-26883251	NR_026793
33	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
34	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
35	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
36	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840

No data

Variant related genes	Relation type
ENSG00000236894	TF binding region
LINC00202-2	TF binding region
LINC00264	TF binding region
ENSG00000234296	TF binding region
ENSG00000236894	CpG island
LINC00202-2	CpG island
LINC00264	CpG island
ENSG00000234296	CpG island
DNMT1	miRNA target sites
PDGFRA	miRNA target sites
ZNF365	miRNA target sites
ZNF367	miRNA target sites

Extended variants
information (count: 4480 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:4480 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75237345	chr10:26861003-26861004	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs79720133	chr10:26861006-26861007	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs373836059	chr10:26861025-26861026	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs557447311	chr10:26861031-26861032	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs577291329	chr10:26861041-26861042	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs539650457	chr10:26861155-26861156	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs542967351	chr10:26861159-26861160	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs113115768	chr10:26861160-26861161	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs556678635	chr10:26861163-26861164	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs576706514	chr10:26861181-26861182	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs144481827	chr10:26861228-26861229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs787016	chr10:26861229-26861230	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs139012192	chr10:26861230-26861231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376040585	chr10:26861238-26861239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201365961	chr10:26861267-26861268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199631515	chr10:26861282-26861283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200786375	chr10:26861285-26861286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202002434	chr10:26861291-26861292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114444442	chr10:26861346-26861347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77858718	chr10:26861353-26861354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72805230	chr10:26861384-26861385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72805231	chr10:26861394-26861395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562095446	chr10:26861395-26861396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72805232	chr10:26861416-26861417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78594617	chr10:26861455-26861456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187115529	chr10:26861469-26861470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76636189	chr10:26861479-26861480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564572034	chr10:26861491-26861492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75048053	chr10:26861500-26861501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200800101	chr10:26861560-26861561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191920615	chr10:26861568-26861569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563494452	chr10:26861598-26861599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149312961	chr10:26861627-26861628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200915669	chr10:26861628-26861629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375991266	chr10:26861649-26861650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74128357	chr10:26861676-26861677	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75037112	chr10:26861683-26861684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370409358	chr10:26861705-26861706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35801387	chr10:26861706-26861707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75429155	chr10:26861707-26861708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs59453295	chr10:26861726-26861727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373415671	chr10:26861727-26861728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11015181	chr10:26861730-26861731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565604661	chr10:26861747-26861748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183773964	chr10:26861762-26861763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114994494	chr10:26861769-26861770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201110926	chr10:26861780-26861781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10829028	chr10:26861784-26861785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571020844	chr10:26861813-26861814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10829029	chr10:26861828-26861829	Weak transcription Strong transcription	n/a	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:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26839800-26861200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr10:26840200-26863200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:26845400-26863000	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr10:26846400-26861600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr10:26846800-26861200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr10:26846800-26863000	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr10:26848200-26861000	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr10:26848400-26863000	Strong transcription	Fetal Thymus	thymus
9	chr10:26856400-26864000	Weak transcription	Pancreas	Pancrea
10	chr10:26857600-26880200	Weak transcription	Adipose Nuclei	Adipose
11	chr10:26858400-26861200	ZNF genes & repeats	Dnd41	blood
12	chr10:26858400-26879400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr10:26859000-26861000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:26859000-26862200	Weak transcription	GM12878-XiMat	blood
15	chr10:26859400-26861000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:26859600-26861000	ZNF genes & repeats	Primary B cells from cord blood	blood
17	chr10:26859600-26861000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
18	chr10:26859600-26861200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr10:26859800-26861000	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr10:26859800-26861000	Enhancers	Liver	Liver
21	chr10:26860000-26861000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
22	chr10:26860000-26861200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:26860200-26861000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:26860600-26861000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
25	chr10:26860800-26861000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:26860800-26862000	Weak transcription	Thymus	Thymus
27	chr10:26860800-26862000	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr10:26860800-26862200	Weak transcription	Primary T cells from cord blood	blood
29	chr10:26860800-26862600	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr10:26860800-26863000	Strong transcription	Primary hematopoietic stem cells	blood
31	chr10:26860800-26881200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr10:26861000-26862000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:26861000-26862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:26861000-26862600	Strong transcription	Primary B cells from cord blood	blood
36	chr10:26861000-26862600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr10:26861000-26862800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr10:26861000-26864200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr10:26861000-26864200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr10:26861000-26864200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:26861000-26874400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr10:26861200-26862000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr10:26861200-26862000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr10:26861200-26862600	Weak transcription	Dnd41	blood
46	chr10:26861200-26872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr10:26861600-26862000	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr10:26862000-26862200	Enhancers	H1 Cell Line	embryonic stem cell

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