Variant report

Variant	esv3363674
Chromosome Location	chr10:26878155-26930279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:552)
Chromatin interactive
region (count:6)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
4	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
5	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
7	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
8	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
9	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
10	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
11	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
14	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
15	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
16	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
17	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
18	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
19	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
20	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
21	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
22	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
23	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr10:26883116-26883294	GM12878	blood:	n/a	n/a
25	CTCF	chr10:26895330-26895646	HUVEC	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
26	CTCF	chr10:26895320-26895470	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr10:26895777-26895832	Lung_OC	lung:	n/a	n/a
28	CTCF	chr10:26895482-26895527	GM20000	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
29	CTCF	chr10:26916320-26916470	GM06990	blood:	n/a	n/a
30	CTCF	chr10:26916300-26916450	HRE	kidney:	n/a	n/a
31	CTCF	chr10:26908392-26908453	GM20000	blood:	n/a	n/a
32	CTCF	chr10:26916360-26916510	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr10:26916408-26916538	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:26896040-26896190	GM12866	blood:	n/a	chr10:26896061-26896069
35	CTCF	chr10:26895300-26895450	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr10:26916380-26916530	Caco-2	colon:	n/a	n/a
37	CTCF	chr10:26895420-26895570	HBMEC	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
38	CTCF	chr10:26916411-26916452	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr10:26916345-26916538	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr10:26916360-26916510	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr10:26895320-26895470	NHEK	skin:	n/a	n/a
42	CTCF	chr10:26895400-26895550	GM12878	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
43	CTCF	chr10:26916401-26916543	Fibrobl	skin:	n/a	n/a
44	CTCF	chr10:26916371-26916569	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr10:26895320-26895470	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr10:26895380-26895612	Kidney_OC	kidney:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
47	CTCF	chr10:26916280-26916430	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr10:26895560-26895710	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr10:26892329-26892425	GM19239	blood:	n/a	n/a
50	CTCF	chr10:26926839-26926880	MCF-7	breast:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26883079-26883129	AoSMC	blood vessel:	n/a
2	chr10:26883165-26883215	HRE	kidney:	n/a
3	chr10:26911451-26911501	K562	blood:	n/a
4	chr10:26883079-26883129	AoSMC	blood vessel:	n/a
5	chr10:26883165-26883215	HRE	kidney:	n/a
6	chr10:26911451-26911501	K562	blood:	n/a
7	chr10:26911451-26911501	HepG2	liver:	n/a
8	chr10:26911186-26911236	NB4	blood:	n/a
9	chr10:26911451-26911501	PFSK-1	brain:	n/a
10	chr10:26883079-26883129	Hepatocyte	liver:	n/a
11	chr10:26883079-26883129	MCF-7	breast:	n/a
12	chr10:26881860-26881910	K562	blood:	n/a
13	chr10:26883165-26883215	SK-N-SH	brain:	n/a
14	chr10:26911451-26911501	RPTEC	kidney:	n/a
15	chr10:26878629-26878679	GM19239	blood:	n/a
16	chr10:26878632-26878682	GM12878	blood:	n/a
17	chr10:26878627-26878677	AG09319	gingival:	n/a
18	chr10:26883079-26883129	H1-hESC	embryonic stem cell:	embryo
19	chr10:26878632-26878682	Hepatocyte	liver:	n/a
20	chr10:26911186-26911236	SK-N-SH_RA	brain:	n/a
21	chr10:26911186-26911236	HCM	heart:	n/a
22	chr10:26878627-26878677	RPTEC	kidney:	n/a
23	chr10:26878629-26878679	HCPEpiC	choroid plexus:	n/a
24	chr10:26878632-26878682	AoSMC	blood vessel:	n/a
25	chr10:26878627-26878677	HCM	heart:	n/a
26	chr10:26878629-26878679	HUVEC	blood vessel:	n/a
27	chr10:26878629-26878679	GM12891	blood:	n/a
28	chr10:26881860-26881910	H1-hESC	embryonic stem cell:	embryo
29	chr10:26883165-26883215	AG04450	lung:	fetal
30	chr10:26878627-26878677	GM12878	blood:	n/a
31	chr10:26883165-26883215	GM12891	blood:	n/a
32	chr10:26883079-26883129	BJ	skin:	n/a
33	chr10:26878629-26878679	LNCaP	prostate:	n/a
34	chr10:26883165-26883215	CMK	blood:	n/a
35	chr10:26883165-26883215	NB4	blood:	n/a
36	chr10:26881860-26881910	NHBE	bronchial:	n/a
37	chr10:26911451-26911501	BE2_C	brain:	n/a
38	chr10:26883013-26883063	Hela-S3	cervix:	n/a
39	chr10:26878629-26878679	SK-N-SH_RA	brain:	n/a
40	chr10:26878629-26878679	Jurkat	blood:	n/a
41	chr10:26883013-26883063	HMEC	breast:	n/a
42	chr10:26881860-26881910	SAEC	small airway:	n/a
43	chr10:26883013-26883063	SAEC	small airway:	n/a
44	chr10:26911186-26911236	HNPCEpiC	eye:	n/a
45	chr10:26878627-26878677	ECC-1	luminal epithelium:	n/a
46	chr10:26878627-26878677	LNCaP	prostate:	n/a
47	chr10:26911451-26911501	MCF10A-Er-Src	breast:	n/a
48	chr10:26878627-26878677	HRPEpiC	eye:	n/a
49	chr10:26911451-26911501	SKMC	muscle:	n/a
50	chr10:26878632-26878682	ECC-1	luminal epithelium:	n/a

(count:6 , 50 per page) page: 1

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

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
2	lnc-APBB1IP-1	chr10:26881779-26882156	XLOC_008419
3	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
4	lnc-PDSS1-1	chr10:26882863-26883251	NR_026793
5	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
6	lnc-PDSS1-1	chr10:26880239-26880342	NR_026793
7	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
8	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
9	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
10	lnc-PDSS1-1	chr10:26879025-26879266	NONHSAT011840
11	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
12	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
13	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
14	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
15	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
16	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
17	lnc-PDSS1-1	chr10:26881779-26881895	NR_026793
18	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
19	lnc-PDSS1-1	chr10:26878794-26879266	NR_026793
20	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
21	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
22	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
23	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
24	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
25	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
26	lnc-APBB1IP-1	chr10:26879064-26879266	XLOC_008419

No data

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

Extended variants
information (count: 2783 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2783 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2995479	chr10:26878169-26878170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374528360	chr10:26878185-26878186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368594837	chr10:26878197-26878198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563992014	chr10:26878217-26878218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374087348	chr10:26878227-26878228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117794413	chr10:26878234-26878235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368987573	chr10:26878266-26878267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549351078	chr10:26878299-26878300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368088722	chr10:26878304-26878305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528977491	chr10:26878315-26878316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2253265	chr10:26878338-26878339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568572805	chr10:26878349-26878350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191934529	chr10:26878388-26878389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201160644	chr10:26878396-26878397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35178820	chr10:26878419-26878420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548133344	chr10:26878442-26878443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571122750	chr10:26878444-26878445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202078014	chr10:26878449-26878450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539874805	chr10:26878467-26878468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556573427	chr10:26878481-26878482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372817036	chr10:26878485-26878486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376995817	chr10:26878488-26878489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369605642	chr10:26878492-26878493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12241063	chr10:26878507-26878508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs117217799	chr10:26878512-26878513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148001768	chr10:26878521-26878522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572148500	chr10:26878528-26878529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540797606	chr10:26878532-26878533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557665685	chr10:26878550-26878551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577494384	chr10:26878552-26878553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543060837	chr10:26878556-26878557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141654779	chr10:26878562-26878563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528842611	chr10:26878565-26878566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542363949	chr10:26878566-26878567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368429312	chr10:26878568-26878569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113249721	chr10:26878597-26878598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553095179	chr10:26878612-26878613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2995478	chr10:26878624-26878625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs116232717	chr10:26878629-26878630	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs571187594	chr10:26878630-26878631	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs17529585	chr10:26878632-26878633	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550189075	chr10:26878656-26878657	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs569959588	chr10:26878659-26878660	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs373028546	chr10:26878660-26878661	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs555600932	chr10:26878662-26878663	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs75830342	chr10:26878669-26878670	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs2985464	chr10:26878671-26878672	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs534537486	chr10:26878672-26878673	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs386742147	chr10:26878691-26878692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2477267	chr10:26878692-26878693	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:348 , 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	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr10:26862400-26882400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr10:26863000-26879200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr10:26864600-26880400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr10:26864800-26881800	Weak transcription	Primary B cells from cord blood	blood
13	chr10:26864800-26882800	Weak transcription	Fetal Thymus	thymus
14	chr10:26865000-26884600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:26867200-26884000	Weak transcription	Right Atrium	heart
16	chr10:26872400-26883000	Weak transcription	Gastric	stomach
17	chr10:26875600-26880800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr10:26875600-26881800	Weak transcription	Thymus	Thymus
19	chr10:26875600-26882800	Weak transcription	Spleen	Spleen
20	chr10:26876000-26879200	Weak transcription	Primary T cells from cord blood	blood
21	chr10:26876200-26880200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr10:26876200-26882600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr10:26878800-26884600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr10:26879000-26888400	Weak transcription	Liver	Liver
25	chr10:26879200-26880400	Strong transcription	Primary T cells from cord blood	blood
26	chr10:26879200-26881200	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr10:26879400-26881000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr10:26880200-26881000	Strong transcription	Adipose Nuclei	Adipose
29	chr10:26880200-26883400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr10:26880400-26881000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:26880400-26887400	Weak transcription	Primary T cells from cord blood	blood
32	chr10:26880800-26881400	Strong transcription	Primary B cells from peripheral blood	blood
33	chr10:26881000-26881800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr10:26881000-26882600	Weak transcription	Adipose Nuclei	Adipose
35	chr10:26881000-26887400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr10:26881200-26882200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr10:26881200-26883200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr10:26881400-26888000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr10:26881800-26882400	Strong transcription	Thymus	Thymus
40	chr10:26881800-26883200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr10:26882200-26883200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr10:26882400-26882600	Weak transcription	Thymus	Thymus
43	chr10:26882600-26882800	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr10:26882600-26883000	Enhancers	Primary hematopoietic stem cells	blood
45	chr10:26882600-26883200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:26882600-26883200	ZNF genes & repeats	Thymus	Thymus
47	chr10:26882800-26883000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr10:26882800-26883000	Genic enhancers	Fetal Thymus	thymus
49	chr10:26882800-26883200	Enhancers	Spleen	Spleen
50	chr10:26882800-26883400	Active TSS	ES-I3 Cell Line	embryonic stem cell

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