Variant report

Variant	nsv520012
Chromosome Location	chr3:136088038-136314119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1175)
CpG islands
(count:183)
Chromatin interactive
region (count:67)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136219790-136219934	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136110571-136110781	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:136265535-136265813	K562	blood:	n/a	n/a
4	ARID3A	chr3:136217754-136218232	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:136295376-136295960	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:136264594-136264721	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:136221984-136222240	HepG2	liver:	n/a	n/a
8	ATF1	chr3:136227712-136227915	K562	blood:	n/a	n/a
9	ATF1	chr3:136296681-136297004	K562	blood:	n/a	n/a
10	BACH1	chr3:136288309-136288380	K562	blood:	n/a	n/a
11	BATF	chr3:136303620-136303859	GM12878	blood:	n/a	n/a
12	BCLAF1	chr3:136110406-136110854	GM12878	blood:	n/a	n/a
13	BCLAF1	chr3:136266136-136266529	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:136305498-136305790	HepG2	liver:	n/a	n/a
15	BHLHE40	chr3:136266318-136266353	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:136217855-136218178	HepG2	liver:	n/a	n/a
17	BHLHE40	chr3:136283473-136283478	GM12878	blood:	n/a	n/a
18	BRCA1	chr3:136207496-136207508	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr3:136271579-136271619	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr3:136174937-136175405	K562	blood:	n/a	n/a
21	CBX3	chr3:136251284-136251617	K562	blood:	n/a	n/a
22	CBX3	chr3:136176200-136176544	K562	blood:	n/a	n/a
23	CBX3	chr3:136296572-136297082	K562	blood:	n/a	n/a
24	CBX3	chr3:136175060-136175369	K562	blood:	n/a	n/a
25	CBX3	chr3:136175073-136175489	HCT-116	colon:	n/a	n/a
26	CCNT2	chr3:136155958-136156415	K562	blood:	n/a	n/a
27	CCNT2	chr3:136153373-136153573	K562	blood:	n/a	n/a
28	CCNT2	chr3:136296609-136296909	K562	blood:	n/a	n/a
29	CEBPB	chr3:136221983-136222211	HepG2	liver:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
30	CEBPB	chr3:136217905-136218295	HepG2	liver:	n/a	chr3:136218083-136218094
31	CEBPB	chr3:136165724-136165729	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:136260862-136261149	IMR90	lung:	n/a	n/a
33	CEBPB	chr3:136217816-136218295	HepG2	liver:	n/a	chr3:136218083-136218094
34	CEBPB	chr3:136313200-136313398	HepG2	liver:	n/a	chr3:136313263-136313274 chr3:136313265-136313276
35	CEBPB	chr3:136153226-136153572	K562	blood:	n/a	n/a
36	CEBPB	chr3:136111448-136111691	HepG2	liver:	n/a	chr3:136111559-136111570
37	CEBPB	chr3:136125741-136126117	A549	lung:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
38	CEBPB	chr3:136222045-136222259	H1-hESC	embryonic stem cell:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
39	CEBPB	chr3:136125640-136126115	A549	lung:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
40	CEBPB	chr3:136125625-136125970	MCF-7	breast:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
41	CEBPB	chr3:136125742-136126113	HepG2	liver:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
42	CEBPB	chr3:136195128-136195532	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:136111445-136111697	H1-hESC	embryonic stem cell:	n/a	chr3:136111559-136111570
44	CEBPB	chr3:136111383-136111737	IMR90	lung:	n/a	chr3:136111559-136111570
45	CEBPB	chr3:136312366-136312485	A549	lung:	n/a	chr3:136312422-136312433 chr3:136312422-136312435 chr3:136312424-136312435
46	CEBPB	chr3:136171262-136171415	Hela-S3	cervix:	n/a	chr3:136171356-136171367
47	CEBPB	chr3:136221930-136222301	HepG2	liver:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
48	CEBPB	chr3:136111498-136111599	HepG2	liver:	n/a	chr3:136111559-136111570
49	CEBPB	chr3:136195158-136195533	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:136125682-136126107	MCF-7	breast:	n/a	chr3:136125860-136125873 chr3:136125924-136125935

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136231858-136231908	GM12878	blood:	n/a
2	chr3:136194317-136194367	IMR90	lung:	fetal
3	chr3:136231858-136231908	AG04449	skin:	fetal
4	chr3:136194317-136194367	HRCEpiC	kidney:	n/a
5	chr3:136192388-136192438	AG04449	skin:	fetal
6	chr3:136192388-136192438	HRCEpiC	kidney:	n/a
7	chr3:136192388-136192438	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:136231858-136231908	HRPEpiC	eye:	n/a
9	chr3:136192388-136192438	NB4	blood:	n/a
10	chr3:136192388-136192438	U87	brain:	n/a
11	chr3:136194317-136194367	NB4	blood:	n/a
12	chr3:136194317-136194367	H1-hESC	embryonic stem cell:	embryo
13	chr3:136192388-136192438	ECC-1	luminal epithelium:	n/a
14	chr3:136194317-136194367	AoSMC	blood vessel:	n/a
15	chr3:136231858-136231908	U87	brain:	n/a
16	chr3:136192388-136192438	BE2_C	brain:	n/a
17	chr3:136231858-136231908	HMEC	breast:	n/a
18	chr3:136194317-136194367	SAEC	small airway:	n/a
19	chr3:136231858-136231908	Caco-2	colon:	n/a
20	chr3:136192388-136192438	HIPEpiC	eye:	n/a
21	chr3:136192388-136192438	HUVEC	blood vessel:	n/a
22	chr3:136231858-136231908	Hepatocyte	liver:	n/a
23	chr3:136192388-136192438	Caco-2	colon:	n/a
24	chr3:136231858-136231908	ProgFib	skin:	n/a
25	chr3:136192388-136192438	AG09309	skin:	n/a
26	chr3:136192388-136192438	T-47D	breast:	n/a
27	chr3:136231858-136231908	H1-hESC	embryonic stem cell:	embryo
28	chr3:136192388-136192438	ovcar-3	ovarian:	n/a
29	chr3:136231858-136231908	AG10803	skin:	n/a
30	chr3:136192388-136192438	GM12892	blood:	n/a
31	chr3:136194317-136194367	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:136192388-136192438	GM12891	blood:	n/a
33	chr3:136192388-136192438	IMR90	lung:	fetal
34	chr3:136192388-136192438	AG09319	gingival:	n/a
35	chr3:136231858-136231908	HEEpiC	esophagus:	n/a
36	chr3:136192388-136192438	SAEC	small airway:	n/a
37	chr3:136231858-136231908	NHDF-neo	bronchial:	n/a
38	chr3:136194317-136194367	BE2_C	brain:	n/a
39	chr3:136192388-136192438	Hela-S3	cervix:	n/a
40	chr3:136194317-136194367	HEEpiC	esophagus:	n/a
41	chr3:136194317-136194367	HL-60	blood:	n/a
42	chr3:136194317-136194367	SK-N-SH_RA	brain:	n/a
43	chr3:136192388-136192438	HCM	heart:	n/a
44	chr3:136192388-136192438	AG04450	lung:	fetal
45	chr3:136192388-136192438	A549	lung:	n/a
46	chr3:136194317-136194367	HEK293	kidney:	embryo
47	chr3:136231858-136231908	HAEpiC	amniotic membrane:	n/a
48	chr3:136192388-136192438	HRE	kidney:	n/a
49	chr3:136194317-136194367	MCF-7	breast:	n/a
50	chr3:136231858-136231908	T-47D	breast:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:135954886..135956782-chr3:136102988..136105563,2	MCF-7	breast:
2	chr3:136168950..136171423-chr3:136205433..136206933,2	K562	blood:
3	chr3:136110282..136111199-chr3:136732444..136733352,7	K562	blood:
4	chr3:136263152..136267364-chr3:136469698..136472182,6	MCF-7	breast:
5	chr3:136262189..136267900-chr3:136469121..136472269,13	MCF-7	breast:
6	chr3:136264257..136265039-chr3:136470501..136471464,2	MCF-7	breast:
7	chr3:136288919..136291137-chr3:136468719..136471296,3	MCF-7	breast:
8	chr3:136223066..136225762-chr3:136237795..136239369,2	MCF-7	breast:
9	chr3:136233567..136235148-chr3:136468458..136469958,2	K562	blood:
10	chr3:136279189..136281857-chr3:136298738..136300966,2	MCF-7	breast:
11	chr3:136281931..136284353-chr3:136295521..136297415,2	K562	blood:
12	chr3:136268066..136271170-chr3:136469546..136471486,3	MCF-7	breast:
13	chr3:136110218..136111115-chr3:136470727..136471338,4	MCF-7	breast:
14	chr3:136237342..136239151-chr3:136470510..136472888,2	MCF-7	breast:
15	chr3:136226210..136226915-chr3:136470643..136471376,2	MCF-7	breast:
16	chr3:136280347..136282243-chr3:136470576..136472647,2	K562	blood:
17	chr3:136313460..136316433-chr3:136321833..136323832,2	MCF-7	breast:
18	chr3:136264021..136266298-chr3:136470657..136471752,36	MCF-7	breast:
19	chr3:136296495..136297649-chr3:136470600..136471459,4	MCF-7	breast:
20	chr3:136263091..136265454-chr3:136470690..136473476,4	K562	blood:
21	chr3:136264546..136265090-chr3:136732553..136733310,2	MCF-7	breast:
22	chr3:136264451..136265000-chr3:136732487..136733381,2	MCF-7	breast:
23	chr3:136286281..136288861-chr3:136469749..136473421,4	K562	blood:
24	chr3:136146516..136149164-chr3:136151874..136154326,2	K562	blood:
25	chr3:136265553..136266283-chr3:136470816..136471681,5	MCF-7	breast:
26	chr3:136166580..136169214-chr3:136176961..136178739,2	MCF-7	breast:
27	chr3:136295071..136296962-chr3:136469759..136471295,2	K562	blood:
28	chr3:135793753..135796262-chr3:136127645..136129401,2	K562	blood:
29	chr3:136309415..136311669-chr3:136473283..136476207,2	K562	blood:
30	chr3:136206783..136208726-chr3:136470130..136472323,2	MCF-7	breast:
31	chr3:136279189..136281857-chr3:136298738..136300966,2	MCF-7	breast:
32	chr3:135914471..135916410-chr3:136223365..136225971,2	MCF-7	breast:
33	chr3:136162413..136165672-chr3:136470682..136473383,3	MCF-7	breast:
34	chr3:136282532..136284441-chr3:136285201..136287062,2	MCF-7	breast:
35	chr3:136274473..136277671-chr3:136469304..136472148,3	K562	blood:
36	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
37	chr3:136257661..136259575-chr3:136470502..136472462,3	MCF-7	breast:
38	chr3:136216747..136218980-chr3:136221671..136224312,2	K562	blood:
39	chr3:136309554..136311362-chr3:136314085..136316749,2	K562	blood:
40	chr3:136296430..136297424-chr3:136470742..136471664,7	MCF-7	breast:
41	chr3:136212773..136214378-chr3:136219138..136220925,2	K562	blood:
42	chr3:136168950..136171423-chr3:136205433..136206933,2	K562	blood:
43	chr3:136277326..136280102-chr3:136471685..136473348,2	MCF-7	breast:
44	chr3:136108896..136113105-chr3:136468716..136472551,4	K562	blood:
45	chr3:136212773..136214378-chr3:136219138..136220925,2	K562	blood:
46	chr3:136110078..136111159-chr3:136470754..136471561,13	MCF-7	breast:
47	chr3:136208388..136211090-chr3:136467197..136470066,2	K562	blood:
48	chr3:136166580..136169214-chr3:136176961..136178739,2	MCF-7	breast:
49	chr3:136261604..136263396-chr3:136467886..136469461,2	K562	blood:
50	chr3:136309554..136311362-chr3:136314085..136316749,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-1284P	TF binding region
RNY4P4	TF binding region
STAG1	TF binding region
RNU6-1284P	CpG island
RNY4P4	CpG island
STAG1	CpG island
ENSG00000118007	chromatin interactions
ENSG00000200571	chromatin interactions
ENSG00000261758	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 9065 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9065 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9860801	chr3:136088038-136088039	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549716315	chr3:136088050-136088051	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs143784838	chr3:136088080-136088081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377654737	chr3:136088132-136088133	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs370481137	chr3:136088167-136088168	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs116779564	chr3:136088173-136088174	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs530681201	chr3:136088211-136088212	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550780490	chr3:136088265-136088266	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569756987	chr3:136088284-136088285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138784822	chr3:136088308-136088309	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538745883	chr3:136088327-136088328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532904030	chr3:136088396-136088397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546298525	chr3:136088415-136088416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566185971	chr3:136088429-136088430	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs148964430	chr3:136088442-136088443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142074826	chr3:136088490-136088491	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543562788	chr3:136088502-136088503	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565855628	chr3:136088540-136088541	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191384750	chr3:136088548-136088549	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571612825	chr3:136088551-136088552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114537935	chr3:136088620-136088621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538133315	chr3:136088647-136088648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558374871	chr3:136088668-136088669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183569651	chr3:136088695-136088696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147027480	chr3:136088716-136088717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540785847	chr3:136088810-136088811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149756744	chr3:136088891-136088892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554309902	chr3:136088908-136088909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376343922	chr3:136088920-136088921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372865777	chr3:136088922-136088923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374922817	chr3:136088925-136088926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71157375	chr3:136088926-136088927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377244638	chr3:136088927-136088928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574154274	chr3:136088934-136088935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116551710	chr3:136088959-136088960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562329658	chr3:136088966-136088967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562723723	chr3:136088971-136088972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534483647	chr3:136089021-136089022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530882831	chr3:136089070-136089071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371885694	chr3:136089072-136089073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201767139	chr3:136089083-136089084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544171388	chr3:136089132-136089133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533759660	chr3:136089161-136089162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116121455	chr3:136089162-136089163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532965491	chr3:136089174-136089175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376242244	chr3:136089188-136089189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190541727	chr3:136089194-136089195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182376913	chr3:136089207-136089208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528942240	chr3:136089224-136089225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147216405	chr3:136089249-136089250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:3076 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136043400-136098600	Weak transcription	Fetal Brain Male	brain
2	chr3:136047600-136098000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr3:136054600-136172000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr3:136055600-136100800	Weak transcription	Spleen	Spleen
5	chr3:136063400-136139000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr3:136063400-136139000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:136063600-136097000	Weak transcription	Colonic Mucosa	Colon
8	chr3:136063600-136105600	Weak transcription	Gastric	stomach
9	chr3:136063600-136110600	Weak transcription	Small Intestine	intestine
10	chr3:136063600-136139200	Weak transcription	Pancreas	Pancrea
11	chr3:136063800-136095200	Weak transcription	Lung	lung
12	chr3:136065400-136097200	Weak transcription	HepG2	liver
13	chr3:136067600-136109000	Weak transcription	HUVEC	blood vessel
14	chr3:136068600-136103800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr3:136069400-136121200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr3:136069600-136107400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr3:136069600-136138800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr3:136069600-136139400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:136069800-136088800	Weak transcription	HMEC	breast
20	chr3:136069800-136106600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr3:136069800-136118800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:136069800-136159600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr3:136070400-136095000	Weak transcription	NH-A	brain
24	chr3:136070600-136101000	Weak transcription	Right Ventricle	heart
25	chr3:136070600-136105800	Weak transcription	Psoas Muscle	Psoas
26	chr3:136070800-136095200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr3:136070800-136096800	Weak transcription	Colon Smooth Muscle	Colon
28	chr3:136070800-136096800	Weak transcription	HSMMtube	muscle
29	chr3:136070800-136099600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr3:136070800-136112200	Weak transcription	Aorta	Aorta
31	chr3:136070800-136121400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:136072600-136098800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:136072800-136097000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr3:136072800-136100400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:136073000-136093800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr3:136075000-136137800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr3:136075400-136093600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:136075400-136093800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr3:136075400-136108000	Weak transcription	Fetal Brain Female	brain
40	chr3:136075600-136094200	Weak transcription	Left Ventricle	heart
41	chr3:136075600-136097000	Weak transcription	Fetal Lung	lung
42	chr3:136075600-136105800	Weak transcription	Ovary	ovary
43	chr3:136075800-136094200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr3:136075800-136099000	Weak transcription	Fetal Muscle Leg	muscle
45	chr3:136075800-136160200	Weak transcription	Brain Germinal Matrix	brain
46	chr3:136076600-136088800	Strong transcription	Dnd41	blood
47	chr3:136078200-136096000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr3:136079400-136174200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:136081200-136093600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:136081200-136118800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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