Variant report

Variant	esv3442075
Chromosome Location	chr10:26884284-26944645
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:916)
Chromatin interactive
region (count:8)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26917389-26917782	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	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
7	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
8	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
9	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
10	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
13	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
14	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
15	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
17	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
18	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
19	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
20	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
21	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
22	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:26916380-26916530	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr10:26937392-26937404	GM10248	blood:	n/a	n/a
25	CTCF	chr10:26895162-26895826	SK-N-SH	brain:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
26	CTCF	chr10:26911360-26911510	SAEC	small airway:	n/a	chr10:26911461-26911474
27	CTCF	chr10:26895400-26895690	AG10803	skin:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
28	CTCF	chr10:26916360-26916510	GM12875	blood:	n/a	n/a
29	CTCF	chr10:26936620-26936770	HMEC	breast:	n/a	n/a
30	CTCF	chr10:26916280-26916430	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr10:26936680-26936830	A549	lung:	n/a	n/a
32	CTCF	chr10:26892341-26892412	NHEK	skin:	n/a	n/a
33	CTCF	chr10:26895320-26895470	HAc	cerebellar:	n/a	n/a
34	CTCF	chr10:26895381-26895577	A549	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
35	CTCF	chr10:26895220-26895370	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr10:26895280-26895430	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr10:26895343-26895661	GM12878	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
38	CTCF	chr10:26936680-26936830	GM12864	blood:	n/a	n/a
39	CTCF	chr10:26895286-26895636	Spleen_OC	spleen:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
40	CTCF	chr10:26895330-26895646	HUVEC	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
41	CTCF	chr10:26936678-26936812	GM19240	blood:	n/a	n/a
42	CTCF	chr10:26895320-26895470	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr10:26926824-26926909	GM19239	blood:	n/a	n/a
44	CTCF	chr10:26936740-26936771	LNCaP	prostate:	n/a	n/a
45	CTCF	chr10:26895730-26895782	GM19240	blood:	n/a	n/a
46	CTCF	chr10:26916360-26916510	AG04449	skin:	n/a	n/a
47	CTCF	chr10:26895276-26895715	A549	lung:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
48	CTCF	chr10:26894571-26894583	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr10:26936656-26936835	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:26926839-26926880	MCF-7	breast:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26930863-26930913	HRCEpiC	kidney:	n/a
2	chr10:26930863-26930913	HRCEpiC	kidney:	n/a
3	chr10:26931986-26932036	HEEpiC	esophagus:	n/a
4	chr10:26932036-26932086	IMR90	lung:	fetal
5	chr10:26931986-26932036	BE2_C	brain:	n/a
6	chr10:26930863-26930913	SK-N-SH	brain:	n/a
7	chr10:26931978-26932028	AG10803	skin:	n/a
8	chr10:26931969-26932019	AG09319	gingival:	n/a
9	chr10:26911186-26911236	HRPEpiC	eye:	n/a
10	chr10:26931986-26932036	Hepatocyte	liver:	n/a
11	chr10:26931912-26931962	GM06990	blood:	n/a
12	chr10:26932036-26932086	T-47D	breast:	n/a
13	chr10:26931986-26932036	PFSK-1	brain:	n/a
14	chr10:26931991-26932041	PFSK-1	brain:	n/a
15	chr10:26931731-26931781	U87	brain:	n/a
16	chr10:26932057-26932107	HAEpiC	amniotic membrane:	n/a
17	chr10:26931926-26931976	SK-N-SH_RA	brain:	n/a
18	chr10:26932057-26932107	SK-N-SH	brain:	n/a
19	chr10:26931978-26932028	NHDF-neo	bronchial:	n/a
20	chr10:26942165-26942215	Jurkat	blood:	n/a
21	chr10:26931969-26932019	Hela-S3	cervix:	n/a
22	chr10:26931978-26932028	HEK293	kidney:	embryo
23	chr10:26931794-26931844	NB4	blood:	n/a
24	chr10:26942165-26942215	HepG2	liver:	n/a
25	chr10:26931986-26932036	HCF	heart:	n/a
26	chr10:26932057-26932107	HUVEC	blood vessel:	n/a
27	chr10:26931991-26932041	AoSMC	blood vessel:	n/a
28	chr10:26930863-26930913	AoSMC	blood vessel:	n/a
29	chr10:26911186-26911236	HEK293	kidney:	embryo
30	chr10:26931912-26931962	PANC-1	pancreas:	n/a
31	chr10:26931926-26931976	SK-N-MC	brain:	n/a
32	chr10:26932057-26932107	MCF-7	breast:	n/a
33	chr10:26932036-26932086	A549	lung:	n/a
34	chr10:26932036-26932086	PFSK-1	brain:	n/a
35	chr10:26931986-26932036	Jurkat	blood:	n/a
36	chr10:26930863-26930913	HUVEC	blood vessel:	n/a
37	chr10:26931978-26932028	H1-hESC	embryonic stem cell:	embryo
38	chr10:26942165-26942215	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:26932036-26932086	NT2-D1	testis:	n/a
40	chr10:26931731-26931781	GM19239	blood:	n/a
41	chr10:26931731-26931781	MCF10A-Er-Src	breast:	n/a
42	chr10:26931794-26931844	NHDF-neo	bronchial:	n/a
43	chr10:26931986-26932036	HL-60	blood:	n/a
44	chr10:26911451-26911501	GM12878	blood:	n/a
45	chr10:26930863-26930913	HIPEpiC	eye:	n/a
46	chr10:26931912-26931962	GM12891	blood:	n/a
47	chr10:26932036-26932086	AG09309	skin:	n/a
48	chr10:26932057-26932107	HL-60	blood:	n/a
49	chr10:26930863-26930913	GM12891	blood:	n/a
50	chr10:26942165-26942215	HIPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

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

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
2	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
3	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
4	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
5	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
6	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
7	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840
8	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
9	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
10	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
11	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
12	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
13	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
14	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
15	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
16	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
17	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
18	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
19	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
20	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841

No data

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

Extended variants
information (count: 3118 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:3118 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149040102	chr10:26884287-26884288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371896977	chr10:26884288-26884289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573991658	chr10:26884339-26884340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541847165	chr10:26884350-26884351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560831208	chr10:26884356-26884357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528424605	chr10:26884362-26884363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142059143	chr10:26884373-26884374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530764920	chr10:26884382-26884383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550477854	chr10:26884388-26884389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190525785	chr10:26884389-26884390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117653610	chr10:26884399-26884400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546874684	chr10:26884407-26884408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566478460	chr10:26884409-26884410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183136481	chr10:26884421-26884422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552284934	chr10:26884460-26884461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568838782	chr10:26884485-26884486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542929604	chr10:26884510-26884511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537696870	chr10:26884538-26884539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576869721	chr10:26884549-26884550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371654273	chr10:26884583-26884584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557124072	chr10:26884585-26884586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556473012	chr10:26884588-26884589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573857057	chr10:26884610-26884611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531705111	chr10:26884618-26884619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375795534	chr10:26884619-26884620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553225529	chr10:26884625-26884626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572920366	chr10:26884635-26884636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116175890	chr10:26884638-26884639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543848230	chr10:26884647-26884648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565403254	chr10:26884651-26884652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369495836	chr10:26884667-26884668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575643672	chr10:26884694-26884695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544433734	chr10:26884695-26884696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141395523	chr10:26884732-26884733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185644503	chr10:26884744-26884745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111866331	chr10:26884766-26884767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369357666	chr10:26884832-26884833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560454069	chr10:26884850-26884851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191591719	chr10:26884851-26884852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563915360	chr10:26884870-26884871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182565191	chr10:26884887-26884888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568976229	chr10:26884897-26884898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537555087	chr10:26884914-26884915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547836429	chr10:26884938-26884939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35059808	chr10:26884954-26884955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187696187	chr10:26884988-26884989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539903251	chr10:26884996-26884997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192368075	chr10:26885032-26885033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73594380	chr10:26885065-26885066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573433131	chr10:26885099-26885100	Weak 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:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr10:26865000-26884600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:26878800-26884600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr10:26879000-26888400	Weak transcription	Liver	Liver
9	chr10:26880400-26887400	Weak transcription	Primary T cells from cord blood	blood
10	chr10:26881000-26887400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:26881400-26888000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr10:26882800-26885400	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr10:26883200-26884400	Weak transcription	Thymus	Thymus
14	chr10:26883200-26885000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:26883200-26892800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr10:26883400-26885400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:26883800-26894200	Weak transcription	Fetal Thymus	thymus
18	chr10:26884400-26884800	Enhancers	Thymus	Thymus
19	chr10:26884800-26890200	Weak transcription	Thymus	Thymus
20	chr10:26888400-26888600	Enhancers	Liver	Liver
21	chr10:26888400-26889000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:26890200-26891200	Enhancers	Thymus	Thymus
23	chr10:26891200-26892400	Weak transcription	Thymus	Thymus
24	chr10:26891800-26893200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:26892400-26893600	Enhancers	Thymus	Thymus
26	chr10:26892600-26892800	Flanking Active TSS	A549	lung
27	chr10:26892600-26893800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr10:26892600-26893800	Enhancers	Dnd41	blood
29	chr10:26892800-26893200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr10:26892800-26893400	Enhancers	Primary T cells from cord blood	blood
31	chr10:26892800-26893600	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr10:26892800-26893800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr10:26893000-26893600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr10:26893600-26895600	Weak transcription	Thymus	Thymus
35	chr10:26893800-26894800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr10:26894200-26897600	Enhancers	Fetal Thymus	thymus
37	chr10:26894800-26895000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr10:26894800-26895400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr10:26895600-26897000	Enhancers	Thymus	Thymus
40	chr10:26900000-26900200	Enhancers	Stomach Mucosa	stomach
41	chr10:26900200-26900800	Weak transcription	Stomach Mucosa	stomach
42	chr10:26900800-26901200	Enhancers	Duodenum Mucosa	Duodenum
43	chr10:26900800-26901800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr10:26900800-26902200	Enhancers	Liver	Liver
45	chr10:26900800-26902200	Enhancers	Fetal Intestine Small	intestine
46	chr10:26900800-26902200	Enhancers	Stomach Mucosa	stomach
47	chr10:26901200-26901800	Active TSS	Duodenum Mucosa	Duodenum
48	chr10:26901400-26902000	Enhancers	Fetal Intestine Large	intestine
49	chr10:26901800-26902000	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr10:26901800-26902200	Active TSS	Rectal Mucosa Donor 29	rectum

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