Variant report

Variant	nsv877527
Chromosome Location	chr3:136182053-136310985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:183)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 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	chr3:136264594-136264721	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136221984-136222240	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:136217754-136218232	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:136219790-136219934	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:136265535-136265813	K562	blood:	n/a	n/a
6	ARID3A	chr3:136295376-136295960	HepG2	liver:	n/a	n/a
7	ATF1	chr3:136227712-136227915	K562	blood:	n/a	n/a
8	ATF1	chr3:136296681-136297004	K562	blood:	n/a	n/a
9	BACH1	chr3:136288309-136288380	K562	blood:	n/a	n/a
10	BATF	chr3:136303620-136303859	GM12878	blood:	n/a	n/a
11	BCLAF1	chr3:136266136-136266529	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:136305498-136305790	HepG2	liver:	n/a	n/a
13	BHLHE40	chr3:136283473-136283478	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:136217855-136218178	HepG2	liver:	n/a	n/a
15	BHLHE40	chr3:136266318-136266353	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:136271579-136271619	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:136207496-136207508	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:136296572-136297082	K562	blood:	n/a	n/a
19	CBX3	chr3:136251284-136251617	K562	blood:	n/a	n/a
20	CCNT2	chr3:136296609-136296909	K562	blood:	n/a	n/a
21	CEBPB	chr3:136195143-136195524	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:136217816-136218295	HepG2	liver:	n/a	chr3:136218083-136218094
23	CEBPB	chr3:136263402-136263741	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:136221930-136222301	HepG2	liver:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
25	CEBPB	chr3:136260885-136261135	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:136217905-136218295	HepG2	liver:	n/a	chr3:136218083-136218094
27	CEBPB	chr3:136222045-136222259	H1-hESC	embryonic stem cell:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
28	CEBPB	chr3:136221983-136222211	HepG2	liver:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
29	CEBPB	chr3:136195120-136195455	MCF-7	breast:	n/a	n/a
30	CEBPB	chr3:136195217-136195495	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:136238094-136238382	HepG2	liver:	n/a	chr3:136238219-136238232 chr3:136238219-136238230
32	CEBPB	chr3:136238096-136238380	IMR90	lung:	n/a	chr3:136238219-136238232 chr3:136238219-136238230
33	CEBPB	chr3:136211989-136212302	A549	lung:	n/a	chr3:136212136-136212147
34	CEBPB	chr3:136305548-136305823	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:136195128-136195532	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:136211981-136212301	HepG2	liver:	n/a	chr3:136212136-136212147
37	CEBPB	chr3:136235024-136235335	HepG2	liver:	n/a	chr3:136235163-136235174
38	CEBPB	chr3:136217851-136218336	HepG2	liver:	n/a	chr3:136218083-136218094
39	CEBPB	chr3:136257928-136257954	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:136195172-136195519	K562	blood:	n/a	n/a
41	CEBPB	chr3:136183125-136183740	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:136260862-136261149	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:136217901-136218195	HepG2	liver:	n/a	chr3:136218083-136218094
44	CEBPB	chr3:136235084-136235217	HepG2	liver:	n/a	chr3:136235163-136235174
45	CEBPB	chr3:136195174-136195526	A549	lung:	n/a	n/a
46	CEBPB	chr3:136195158-136195533	IMR90	lung:	n/a	n/a
47	CEBPB	chr3:136260892-136261148	A549	lung:	n/a	n/a
48	CEBPB	chr3:136260874-136261157	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:136221990-136222240	K562	blood:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
50	CEBPB	chr3:136258893-136259079	HepG2	liver:	n/a	chr3:136258988-136259001 chr3:136258988-136258999

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136192388-136192438	PANC-1	pancreas:	n/a
2	chr3:136231858-136231908	IMR90	lung:	fetal
3	chr3:136194317-136194367	Caco-2	colon:	n/a
4	chr3:136192388-136192438	Caco-2	colon:	n/a
5	chr3:136192388-136192438	BE2_C	brain:	n/a
6	chr3:136194317-136194367	NB4	blood:	n/a
7	chr3:136231858-136231908	SKMC	muscle:	n/a
8	chr3:136194317-136194367	GM06990	blood:	n/a
9	chr3:136192388-136192438	HUVEC	blood vessel:	n/a
10	chr3:136192388-136192438	NH-A	brain:	n/a
11	chr3:136231858-136231908	AG04449	skin:	fetal
12	chr3:136194317-136194367	HL-60	blood:	n/a
13	chr3:136231858-136231908	HEEpiC	esophagus:	n/a
14	chr3:136192388-136192438	HNPCEpiC	eye:	n/a
15	chr3:136231858-136231908	HCF	heart:	n/a
16	chr3:136194317-136194367	AG09319	gingival:	n/a
17	chr3:136231858-136231908	GM12892	blood:	n/a
18	chr3:136231858-136231908	NB4	blood:	n/a
19	chr3:136194317-136194367	SK-N-MC	brain:	n/a
20	chr3:136194317-136194367	HCM	heart:	n/a
21	chr3:136231858-136231908	CMK	blood:	n/a
22	chr3:136194317-136194367	HEEpiC	esophagus:	n/a
23	chr3:136194317-136194367	U87	brain:	n/a
24	chr3:136231858-136231908	A549	lung:	n/a
25	chr3:136231858-136231908	SK-N-MC	brain:	n/a
26	chr3:136231858-136231908	BJ	skin:	n/a
27	chr3:136194317-136194367	IMR90	lung:	fetal
28	chr3:136194317-136194367	HRCEpiC	kidney:	n/a
29	chr3:136192388-136192438	IMR90	lung:	fetal
30	chr3:136194317-136194367	GM12892	blood:	n/a
31	chr3:136192388-136192438	HAEpiC	amniotic membrane:	n/a
32	chr3:136192388-136192438	SK-N-MC	brain:	n/a
33	chr3:136194317-136194367	AG10803	skin:	n/a
34	chr3:136231858-136231908	ovcar-3	ovarian:	n/a
35	chr3:136192388-136192438	ECC-1	luminal epithelium:	n/a
36	chr3:136194317-136194367	HRE	kidney:	n/a
37	chr3:136192388-136192438	GM12891	blood:	n/a
38	chr3:136231858-136231908	HIPEpiC	eye:	n/a
39	chr3:136231858-136231908	ECC-1	luminal epithelium:	n/a
40	chr3:136192388-136192438	BJ	skin:	n/a
41	chr3:136194317-136194367	HNPCEpiC	eye:	n/a
42	chr3:136231858-136231908	HCPEpiC	choroid plexus:	n/a
43	chr3:136231858-136231908	HAEpiC	amniotic membrane:	n/a
44	chr3:136231858-136231908	HepG2	liver:	n/a
45	chr3:136192388-136192438	LNCaP	prostate:	n/a
46	chr3:136194317-136194367	BJ	skin:	n/a
47	chr3:136194317-136194367	HIPEpiC	eye:	n/a
48	chr3:136192388-136192438	NHBE	bronchial:	n/a
49	chr3:136231858-136231908	HL-60	blood:	n/a
50	chr3:136192388-136192438	HMEC	breast:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:136263152..136267364-chr3:136469698..136472182,6	MCF-7	breast:
2	chr3:136212773..136214378-chr3:136219138..136220925,2	K562	blood:
3	chr3:136206783..136208726-chr3:136470130..136472323,2	MCF-7	breast:
4	chr3:136288919..136291137-chr3:136468719..136471296,3	MCF-7	breast:
5	chr3:136309554..136311362-chr3:136314085..136316749,2	K562	blood:
6	chr3:136223066..136225762-chr3:136237795..136239369,2	MCF-7	breast:
7	chr3:136282532..136284441-chr3:136285201..136287062,2	MCF-7	breast:
8	chr3:136264178..136265425-chr3:136470257..136471763,14	MCF-7	breast:
9	chr3:136277326..136280102-chr3:136471685..136473348,2	MCF-7	breast:
10	chr3:136265553..136266283-chr3:136470816..136471681,5	MCF-7	breast:
11	chr3:136257661..136259575-chr3:136470502..136472462,3	MCF-7	breast:
12	chr3:136279189..136281857-chr3:136298738..136300966,2	MCF-7	breast:
13	chr3:136233567..136235148-chr3:136468458..136469958,2	K562	blood:
14	chr3:136295071..136296962-chr3:136469759..136471295,2	K562	blood:
15	chr3:136280347..136282243-chr3:136470576..136472647,2	K562	blood:
16	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
17	chr3:136262189..136267900-chr3:136469121..136472269,13	MCF-7	breast:
18	chr3:136223066..136225762-chr3:136237795..136239369,2	MCF-7	breast:
19	chr3:136226210..136226915-chr3:136470643..136471376,2	MCF-7	breast:
20	chr3:136212773..136214378-chr3:136219138..136220925,2	K562	blood:
21	chr3:136216747..136218980-chr3:136221671..136224312,2	K562	blood:
22	chr3:136268066..136271170-chr3:136469546..136471486,3	MCF-7	breast:
23	chr3:136296495..136297649-chr3:136470600..136471459,4	MCF-7	breast:
24	chr3:136208388..136211090-chr3:136467197..136470066,2	K562	blood:
25	chr3:136264021..136266298-chr3:136470657..136471752,36	MCF-7	breast:
26	chr3:136303371..136305169-chr3:136469440..136472893,3	MCF-7	breast:
27	chr3:136275233..136277480-chr3:136465524..136468247,2	K562	blood:
28	chr3:136261604..136263396-chr3:136467886..136469461,2	K562	blood:
29	chr3:136264451..136265000-chr3:136732487..136733381,2	MCF-7	breast:
30	chr3:136281931..136284353-chr3:136295521..136297415,2	K562	blood:
31	chr3:136286281..136288861-chr3:136469749..136473421,4	K562	blood:
32	chr3:136237342..136239151-chr3:136470510..136472888,2	MCF-7	breast:
33	chr3:135914471..135916410-chr3:136223365..136225971,2	MCF-7	breast:
34	chr3:136262930..136265454-chr3:136470250..136473086,3	K562	blood:
35	chr3:136279189..136281857-chr3:136298738..136300966,2	MCF-7	breast:
36	chr3:136264257..136265039-chr3:136470501..136471464,2	MCF-7	breast:
37	chr3:136274473..136277671-chr3:136469304..136472148,3	K562	blood:
38	chr3:136216747..136218980-chr3:136221671..136224312,2	K562	blood:
39	chr3:136281931..136284353-chr3:136295521..136297415,2	K562	blood:
40	chr3:136263091..136265454-chr3:136470690..136473476,4	K562	blood:
41	chr3:136247859..136250822-chr3:136470944..136473511,2	K562	blood:
42	chr3:136224749..136227067-chr3:136470099..136472380,2	K562	blood:
43	chr3:136282532..136284441-chr3:136285201..136287062,2	MCF-7	breast:
44	chr3:136296430..136297424-chr3:136470742..136471664,7	MCF-7	breast:
45	chr3:136309415..136311669-chr3:136473283..136476207,2	K562	blood:
46	chr3:136264546..136265090-chr3:136732553..136733310,2	MCF-7	breast:
47	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
48	chr3:136295071..136298388-chr3:136468846..136472578,3	K562	blood:
49	chr3:136168950..136171423-chr3:136205433..136206933,2	K562	blood:

No data

Variant related genes	Relation type
RNY4P4	TF binding region
STAG1	TF binding region
RNY4P4	CpG island
STAG1	CpG island
ENSG00000118007	chromatin interactions
ENSG00000174579	chromatin interactions
ENSG00000261758	chromatin interactions

Extended variants
information (count: 5247 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5247 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11715257	chr3:136182053-136182054	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72989405	chr3:136182109-136182110	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534531436	chr3:136182121-136182122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186501747	chr3:136182168-136182169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370653024	chr3:136182193-136182194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543859408	chr3:136182195-136182196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373334755	chr3:136182202-136182203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556125751	chr3:136182223-136182224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189812022	chr3:136182259-136182260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140894116	chr3:136182373-136182374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558801263	chr3:136182444-136182445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573525116	chr3:136182445-136182446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377478535	chr3:136182468-136182469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572561686	chr3:136182472-136182473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577422674	chr3:136182497-136182498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555249169	chr3:136182532-136182533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575200458	chr3:136182537-136182538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376115912	chr3:136182544-136182545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530519093	chr3:136182557-136182558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544161873	chr3:136182568-136182569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140989476	chr3:136182577-136182578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369677863	chr3:136182582-136182583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376412221	chr3:136182583-136182584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75444292	chr3:136182586-136182587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185133193	chr3:136182609-136182610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563251202	chr3:136182611-136182612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375928916	chr3:136182612-136182613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150127558	chr3:136182614-136182615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191077240	chr3:136182617-136182618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528363731	chr3:136182631-136182632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372374909	chr3:136182633-136182634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367887280	chr3:136182642-136182643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545847088	chr3:136182708-136182709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536625024	chr3:136182709-136182710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559191684	chr3:136182783-136182784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528240540	chr3:136182797-136182798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547976693	chr3:136182802-136182803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555906754	chr3:136182813-136182814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567951731	chr3:136182827-136182828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371718276	chr3:136182842-136182843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541795312	chr3:136182850-136182851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562033859	chr3:136182880-136182881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550485353	chr3:136182899-136182900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76732302	chr3:136182911-136182912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138677817	chr3:136182930-136182931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538666321	chr3:136182955-136182956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558964040	chr3:136183013-136183014	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566038512	chr3:136183038-136183039	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs61789652	chr3:136183041-136183042	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555185479	chr3:136183053-136183054	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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

Chromatin state (count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136176400-136186000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr3:136176400-136190600	Weak transcription	Gastric	stomach
3	chr3:136176400-136194200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr3:136176400-136194400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr3:136176400-136194400	Weak transcription	HSMM	muscle
6	chr3:136176400-136314200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:136176600-136183400	Weak transcription	Aorta	Aorta
8	chr3:136176600-136190400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:136176600-136195000	Weak transcription	Colon Smooth Muscle	Colon
10	chr3:136176600-136195000	Weak transcription	Spleen	Spleen
11	chr3:136176600-136196600	Weak transcription	HUVEC	blood vessel
12	chr3:136176600-136212000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:136176600-136222800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:136176600-136224200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr3:136176600-136224400	Weak transcription	Brain Hippocampus Middle	brain
16	chr3:136176600-136231800	Weak transcription	Psoas Muscle	Psoas
17	chr3:136176600-136240000	Weak transcription	HMEC	breast
18	chr3:136176600-136260800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr3:136176800-136183000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr3:136176800-136183000	Weak transcription	Right Ventricle	heart
21	chr3:136176800-136183600	Weak transcription	NH-A	brain
22	chr3:136176800-136189800	Weak transcription	Liver	Liver
23	chr3:136176800-136190000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr3:136176800-136190600	Weak transcription	Left Ventricle	heart
25	chr3:136176800-136190600	Weak transcription	Pancreas	Pancrea
26	chr3:136176800-136191600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr3:136176800-136193400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr3:136176800-136193400	Weak transcription	Esophagus	oesophagus
29	chr3:136176800-136193600	Weak transcription	Ovary	ovary
30	chr3:136176800-136194400	Weak transcription	Brain Anterior Caudate	brain
31	chr3:136176800-136194400	Weak transcription	Brain Germinal Matrix	brain
32	chr3:136176800-136194800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:136176800-136205800	Weak transcription	Small Intestine	intestine
34	chr3:136176800-136228000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr3:136176800-136266200	Weak transcription	Hela-S3	cervix
36	chr3:136177000-136183200	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:136177000-136190400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr3:136177000-136191800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:136177200-136183000	Weak transcription	Lung	lung
40	chr3:136177200-136183200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr3:136177200-136236400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr3:136177400-136183000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:136177400-136183000	Weak transcription	Fetal Muscle Leg	muscle
44	chr3:136177400-136183000	Weak transcription	Thymus	Thymus
45	chr3:136177400-136190200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr3:136177400-136190600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr3:136177400-136191600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr3:136177400-136198400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr3:136177600-136182200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:136177600-136183000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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