Variant report

Variant	nsv877679
Chromosome Location	chr3:155128968-155204939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:155130684-155130868	K562	blood:	n/a	n/a
2	BACH1	chr3:155139344-155139381	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr3:155134422-155135082	A549	lung:	n/a	n/a
4	CEBPB	chr3:155154140-155154337	HepG2	liver:	n/a	chr3:155154176-155154189
5	CEBPB	chr3:155134631-155134899	A549	lung:	n/a	n/a
6	CEBPB	chr3:155134595-155134899	A549	lung:	n/a	n/a
7	CEBPB	chr3:155151454-155151614	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:155180490-155180849	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:155181794-155181965	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:155180528-155180764	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:155180589-155180792	K562	blood:	n/a	n/a
12	CEBPB	chr3:155180608-155180815	HepG2	liver:	n/a	n/a
13	CTCF	chr3:155129720-155129870	GM12872	blood:	n/a	n/a
14	CTCF	chr3:155129776-155129898	NHEK	skin:	n/a	n/a
15	CTCF	chr3:155129784-155129908	GM19240	blood:	n/a	n/a
16	CTCF	chr3:155138800-155138950	BE2_C	brain:	n/a	n/a
17	CTCF	chr3:155129760-155129910	GM06990	blood:	n/a	n/a
18	CTCF	chr3:155138687-155139027	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:155138720-155138870	AG10803	skin:	n/a	n/a
20	CTCF	chr3:155138760-155138910	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr3:155138598-155139140	MCF-7	breast:	n/a	n/a
22	CTCF	chr3:155138780-155138930	HepG2	liver:	n/a	n/a
23	CTCF	chr3:155129700-155129850	GM12875	blood:	n/a	n/a
24	CTCF	chr3:155138780-155138930	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr3:155138780-155138930	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr3:155129720-155129870	HMEC	breast:	n/a	n/a
27	CTCF	chr3:155129740-155129890	HepG2	liver:	n/a	n/a
28	CTCF	chr3:155129720-155129870	NB4	blood:	n/a	n/a
29	CTCF	chr3:155129745-155129917	K562	blood:	n/a	n/a
30	CTCF	chr3:155138757-155139032	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr3:155129680-155129830	HCT-116	colon:	n/a	n/a
32	CTCF	chr3:155138779-155138931	HepG2	liver:	n/a	n/a
33	CTCF	chr3:155129760-155129910	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr3:155138616-155139063	K562	blood:	n/a	n/a
35	CTCF	chr3:155138785-155138916	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr3:155129773-155129889	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:155138760-155138910	K562	blood:	n/a	n/a
38	CTCF	chr3:155129763-155129907	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr3:155129730-155129985	K562	blood:	n/a	n/a
40	CTCF	chr3:155129769-155129908	GM12878	blood:	n/a	n/a
41	CTCF	chr3:155129740-155129890	GM12869	blood:	n/a	n/a
42	CTCF	chr3:155129773-155129916	GM12892	blood:	n/a	n/a
43	CTCF	chr3:155129720-155129870	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr3:155138820-155138970	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr3:155129784-155129899	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:155129720-155129870	BE2_C	brain:	n/a	n/a
47	CTCF	chr3:155129740-155129890	RPTEC	kidney:	n/a	n/a
48	CTCF	chr3:155138780-155138930	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr3:155129760-155129910	GM12866	blood:	n/a	n/a
50	CTCF	chr3:155129816-155129865	GM13977	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155198149-155198199	Hela-S3	cervix:	n/a
2	chr3:155200562-155200612	HNPCEpiC	eye:	n/a
3	chr3:155198149-155198199	CMK	blood:	n/a
4	chr3:155139702-155139752	HRCEpiC	kidney:	n/a
5	chr3:155198149-155198199	T-47D	breast:	n/a
6	chr3:155200562-155200612	GM19239	blood:	n/a
7	chr3:155198149-155198199	GM12892	blood:	n/a
8	chr3:155198149-155198199	GM12878	blood:	n/a
9	chr3:155200562-155200612	AG09309	skin:	n/a
10	chr3:155200562-155200612	AG10803	skin:	n/a
11	chr3:155139702-155139752	GM12878	blood:	n/a
12	chr3:155180813-155180863	AG09309	skin:	n/a
13	chr3:155200562-155200612	Hela-S3	cervix:	n/a
14	chr3:155200562-155200612	AG04450	lung:	fetal
15	chr3:155200562-155200612	GM12891	blood:	n/a
16	chr3:155139702-155139752	A549	lung:	n/a
17	chr3:155180813-155180863	GM12878	blood:	n/a
18	chr3:155198149-155198199	Caco-2	colon:	n/a
19	chr3:155198149-155198199	SKMC	muscle:	n/a
20	chr3:155180813-155180863	HCF	heart:	n/a
21	chr3:155198149-155198199	HRE	kidney:	n/a
22	chr3:155198149-155198199	ProgFib	skin:	n/a
23	chr3:155198149-155198199	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:155139702-155139752	PrEC	prostate:	n/a
25	chr3:155200562-155200612	HRCEpiC	kidney:	n/a
26	chr3:155198149-155198199	AG09309	skin:	n/a
27	chr3:155200562-155200612	AoSMC	blood vessel:	n/a
28	chr3:155180813-155180863	H1-hESC	embryonic stem cell:	embryo
29	chr3:155139702-155139752	Hepatocyte	liver:	n/a
30	chr3:155198149-155198199	NB4	blood:	n/a
31	chr3:155180813-155180863	HIPEpiC	eye:	n/a
32	chr3:155180813-155180863	Jurkat	blood:	n/a
33	chr3:155180813-155180863	K562	blood:	n/a
34	chr3:155180813-155180863	GM06990	blood:	n/a
35	chr3:155180813-155180863	SKMC	muscle:	n/a
36	chr3:155180813-155180863	ovcar-3	ovarian:	n/a
37	chr3:155200562-155200612	HMEC	breast:	n/a
38	chr3:155200562-155200612	MCF-7	breast:	n/a
39	chr3:155200562-155200612	Jurkat	blood:	n/a
40	chr3:155198149-155198199	ovcar-3	ovarian:	n/a
41	chr3:155180813-155180863	HAEpiC	amniotic membrane:	n/a
42	chr3:155139702-155139752	T-47D	breast:	n/a
43	chr3:155198149-155198199	ECC-1	luminal epithelium:	n/a
44	chr3:155139702-155139752	Hela-S3	cervix:	n/a
45	chr3:155180813-155180863	Hepatocyte	liver:	n/a
46	chr3:155200562-155200612	T-47D	breast:	n/a
47	chr3:155198149-155198199	BE2_C	brain:	n/a
48	chr3:155139702-155139752	SK-N-MC	brain:	n/a
49	chr3:155198149-155198199	HEK293	kidney:	embryo
50	chr3:155198149-155198199	MCF-7	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:155130861..155132542-chr3:155132605..155134388,2	MCF-7	breast:
2	chr3:155135726..155137467-chr3:155146155..155148179,2	MCF-7	breast:
3	chr3:155134212..155136487-chr3:155137053..155139235,2	MCF-7	breast:
4	chr3:155166382..155168478-chr3:155179446..155181063,2	MCF-7	breast:
5	chr3:155161165..155164024-chr3:155164178..155166734,2	MCF-7	breast:
6	chr3:155178266..155180297-chr3:155313970..155315734,2	K562	blood:
7	chr3:155198984..155201887-chr3:155202554..155204324,2	K562	blood:
8	chr3:155161165..155164024-chr3:155164178..155166734,2	MCF-7	breast:
9	chr3:155130861..155132542-chr3:155132605..155134388,2	MCF-7	breast:
10	chr3:155138815..155140992-chr3:155141903..155144535,2	MCF-7	breast:
11	chr3:155167059..155168776-chr3:155182415..155184760,2	K562	blood:
12	chr3:155140732..155143652-chr3:155144981..155146803,2	MCF-7	breast:
13	chr3:155108548..155110604-chr3:155127196..155130080,2	MCF-7	breast:
14	chr3:155140732..155143652-chr3:155144981..155146803,2	MCF-7	breast:
15	chr3:155130485..155132215-chr3:155138611..155141364,2	K562	blood:
16	chr3:155125953..155128553-chr3:155134009..155136555,2	MCF-7	breast:
17	chr3:155138815..155140992-chr3:155141903..155144535,2	MCF-7	breast:
18	chr3:155135726..155137467-chr3:155146155..155148179,2	MCF-7	breast:
19	chr3:155167059..155168776-chr3:155182415..155184760,2	K562	blood:
20	chr3:155134212..155136487-chr3:155137053..155139235,2	MCF-7	breast:
21	chr3:155130485..155132215-chr3:155138611..155141364,2	K562	blood:
22	chr3:155196848..155198866-chr3:155199886..155201539,2	K562	blood:
23	chr3:155138776..155139298-chr3:155419434..155420178,2	MCF-7	breast:
24	chr3:155196848..155198866-chr3:155199886..155201539,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MME-4	chr3:155204750-155204910	ENSG00000242925.1
2	lnc-MME-3	chr3:155166973-155167214	ENSG00000239508.1
3	lnc-MME-4	chr3:155203592-155203838	ENSG00000242925.1
4	lnc-AC104472.1-2	chr3:155150659-155151187	NONHSAT092835
5	lnc-AC104472.1-2	chr3:155149018-155149435	NONHSAT092835
6	lnc-MME-3	chr3:155174477-155175542	ENSG00000239508.1

No data

Variant related genes	Relation type
PLCH1-AS2	TF binding region
PLCH1-AS1	TF binding region
ENSG00000272096	TF binding region
ENSG00000242152	TF binding region
PLCH1-AS2	CpG island
PLCH1-AS1	CpG island
ENSG00000272096	CpG island
ENSG00000242152	CpG island
ENSG00000239508	chromatin interactions
ENSG00000242925	chromatin interactions

Extended variants
information (count: 2819 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2819 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6802130	chr3:155128968-155128969	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75748295	chr3:155129001-155129002	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs532694859	chr3:155129009-155129010	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs149512694	chr3:155129018-155129019	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs191503420	chr3:155129020-155129021	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs147183947	chr3:155129023-155129024	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs150108320	chr3:155129027-155129028	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs549276665	chr3:155129100-155129101	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140633871	chr3:155129122-155129123	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs386667324	chr3:155129140-155129141	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs6789445	chr3:155129141-155129142	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180735768	chr3:155129142-155129143	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs142923397	chr3:155129151-155129152	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs114715143	chr3:155129152-155129153	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs6802336	chr3:155129161-155129162	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs572319601	chr3:155129178-155129179	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs147427533	chr3:155129187-155129188	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs555246429	chr3:155129217-155129218	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs576317990	chr3:155129299-155129300	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs6440982	chr3:155129323-155129324	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs565326353	chr3:155129331-155129332	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs185016635	chr3:155129348-155129349	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs541577665	chr3:155129408-155129409	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs560347558	chr3:155129429-155129430	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs35512610	chr3:155129439-155129440	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs7612603	chr3:155129440-155129441	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs117052297	chr3:155129457-155129458	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs112975613	chr3:155129463-155129464	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs75653366	chr3:155129533-155129534	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs142510446	chr3:155129565-155129566	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs114516490	chr3:155129591-155129592	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs7637223	chr3:155129643-155129644	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150959128	chr3:155129647-155129648	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs566114223	chr3:155129651-155129652	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs189823515	chr3:155129655-155129656	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs574708554	chr3:155129691-155129692	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs183214750	chr3:155129746-155129747	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs570307120	chr3:155129816-155129817	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs139496318	chr3:155129826-155129827	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs538727858	chr3:155129840-155129841	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs558982153	chr3:155129846-155129847	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs577318425	chr3:155129847-155129848	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs541487981	chr3:155129854-155129855	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs114009595	chr3:155129859-155129860	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs572110228	chr3:155129860-155129861	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs542789083	chr3:155129885-155129886	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs527875413	chr3:155129910-155129911	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs144900109	chr3:155129916-155129917	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs187907172	chr3:155129930-155129931	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs560974786	chr3:155129938-155129939	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	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
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155125800-155134200	Weak transcription	Osteobl	bone
2	chr3:155128200-155130200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:155128800-155129200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:155128800-155129800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr3:155129200-155130200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:155129800-155130600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:155130200-155130600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:155130200-155132800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr3:155130600-155131000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr3:155130600-155131000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:155130600-155131000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:155130600-155131000	Enhancers	K562	blood
13	chr3:155130600-155131200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:155130600-155131200	Enhancers	Duodenum Mucosa	Duodenum
15	chr3:155130600-155131400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr3:155130600-155131400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr3:155130600-155131600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:155130600-155131600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr3:155130600-155131600	Enhancers	Fetal Intestine Large	intestine
20	chr3:155130600-155132400	Enhancers	Fetal Intestine Small	intestine
21	chr3:155130800-155131200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr3:155130800-155131200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:155130800-155131200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:155130800-155131600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:155130800-155131600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr3:155131000-155131600	Enhancers	Stomach Mucosa	stomach
27	chr3:155131000-155135400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:155131000-155138800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr3:155131200-155132800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:155131200-155135000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr3:155131200-155136000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:155131600-155132600	Weak transcription	Fetal Intestine Large	intestine
33	chr3:155131600-155132800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:155132800-155133000	Enhancers	Fetal Intestine Large	intestine
35	chr3:155132800-155133200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:155133200-155135600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:155133600-155136400	Enhancers	HMEC	breast
38	chr3:155133800-155134200	Enhancers	A549	lung
39	chr3:155133800-155135200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:155133800-155135400	Enhancers	NHDF-Ad	bronchial
41	chr3:155134000-155134200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr3:155134000-155135200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr3:155134000-155135600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:155134000-155136000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:155134000-155136000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr3:155134000-155136000	Enhancers	NHEK	skin
47	chr3:155134000-155136400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:155134200-155134600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr3:155134200-155135000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:155134200-155135000	Flanking Active TSS	A549	lung

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