Variant report

Variant	nsv834381
Chromosome Location	chr2:133722671-133897994
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:305)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:133892668-133892866	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:133736400-133736844	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:133897445-133897743	H1-hESC	embryonic stem cell:	n/a	chr2:133897635-133897644 chr2:133897634-133897643
4	BHLHE40	chr2:133770871-133771272	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:133736509-133736513	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:133727257-133727412	GM12878	blood:	n/a	n/a
7	CEBPB	chr2:133792934-133793194	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:133752193-133752411	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:133752159-133752432	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
12	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:133792877-133793234	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:133748918-133749459	HepG2	liver:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
15	CEBPB	chr2:133782590-133782918	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:133808972-133809055	HepG2	liver:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
17	CEBPB	chr2:133888428-133888781	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:133748993-133749121	Hela-S3	cervix:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
19	CEBPB	chr2:133735747-133736076	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:133797776-133798143	IMR90	lung:	n/a	chr2:133797955-133797966
21	CEBPB	chr2:133797821-133798110	A549	lung:	n/a	chr2:133797955-133797966
22	CEBPB	chr2:133797830-133798092	HepG2	liver:	n/a	chr2:133797955-133797966
23	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:133723194-133723273	HepG2	liver:	n/a	chr2:133723220-133723231
25	CEBPB	chr2:133792922-133793196	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
28	CEBPB	chr2:133752167-133752449	A549	lung:	n/a	n/a
29	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
30	CEBPB	chr2:133748166-133748284	A549	lung:	n/a	chr2:133748232-133748243
31	CEBPB	chr2:133897405-133897664	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:133724477-133724677	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:133797903-133797994	H1-hESC	embryonic stem cell:	n/a	chr2:133797955-133797966
35	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:133808875-133809161	IMR90	lung:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
40	CEBPB	chr2:133792973-133793173	A549	lung:	n/a	n/a
41	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
43	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
44	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
46	CEBPB	chr2:133748145-133748354	HepG2	liver:	n/a	chr2:133748232-133748243
47	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
48	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133888263-133888313	T-47D	breast:	n/a
2	chr2:133868449-133868499	SK-N-SH	brain:	n/a
3	chr2:133868449-133868499	RPTEC	kidney:	n/a
4	chr2:133868449-133868499	HCT-116	colon:	n/a
5	chr2:133868449-133868499	GM12878	blood:	n/a
6	chr2:133868449-133868499	PANC-1	pancreas:	n/a
7	chr2:133733241-133733291	SK-N-SH_RA	brain:	n/a
8	chr2:133868449-133868499	HCPEpiC	choroid plexus:	n/a
9	chr2:133868449-133868499	HMEC	breast:	n/a
10	chr2:133888263-133888313	MCF10A-Er-Src	breast:	n/a
11	chr2:133855847-133855897	SAEC	small airway:	n/a
12	chr2:133733241-133733291	PrEC	prostate:	n/a
13	chr2:133855847-133855897	HUVEC	blood vessel:	n/a
14	chr2:133834998-133835048	SK-N-MC	brain:	n/a
15	chr2:133855847-133855897	CMK	blood:	n/a
16	chr2:133733241-133733291	GM06990	blood:	n/a
17	chr2:133733241-133733291	SAEC	small airway:	n/a
18	chr2:133888263-133888313	U87	brain:	n/a
19	chr2:133888263-133888313	MCF-7	breast:	n/a
20	chr2:133855847-133855897	HRCEpiC	kidney:	n/a
21	chr2:133868449-133868499	U87	brain:	n/a
22	chr2:133855847-133855897	HRE	kidney:	n/a
23	chr2:133868449-133868499	HCF	heart:	n/a
24	chr2:133834998-133835048	HepG2	liver:	n/a
25	chr2:133834998-133835048	NB4	blood:	n/a
26	chr2:133855847-133855897	H1-hESC	embryonic stem cell:	embryo
27	chr2:133733241-133733291	HMEC	breast:	n/a
28	chr2:133888263-133888313	GM06990	blood:	n/a
29	chr2:133855847-133855897	AG04449	skin:	fetal
30	chr2:133733241-133733291	Caco-2	colon:	n/a
31	chr2:133733241-133733291	HRE	kidney:	n/a
32	chr2:133834998-133835048	A549	lung:	n/a
33	chr2:133855847-133855897	NB4	blood:	n/a
34	chr2:133733241-133733291	MCF10A-Er-Src	breast:	n/a
35	chr2:133733241-133733291	ProgFib	skin:	n/a
36	chr2:133834998-133835048	AG09309	skin:	n/a
37	chr2:133834998-133835048	PANC-1	pancreas:	n/a
38	chr2:133868449-133868499	HEK293	kidney:	embryo
39	chr2:133834998-133835048	AG04449	skin:	fetal
40	chr2:133733241-133733291	SK-N-SH	brain:	n/a
41	chr2:133868449-133868499	PFSK-1	brain:	n/a
42	chr2:133855847-133855897	HMEC	breast:	n/a
43	chr2:133834998-133835048	BJ	skin:	n/a
44	chr2:133733241-133733291	PANC-1	pancreas:	n/a
45	chr2:133888263-133888313	Jurkat	blood:	n/a
46	chr2:133868449-133868499	H1-hESC	embryonic stem cell:	embryo
47	chr2:133868449-133868499	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:133855847-133855897	BE2_C	brain:	n/a
49	chr2:133834998-133835048	HEK293	kidney:	embryo
50	chr2:133855847-133855897	ProgFib	skin:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133795860..133798019-chr2:133803076..133805297,2	MCF-7	breast:
2	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
3	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
4	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
5	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
6	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
7	chr2:133795860..133798019-chr2:133803076..133805297,2	MCF-7	breast:
8	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
9	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
10	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
11	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
12	chr2:133831745..133832436-chr8:97637034..97637925,2	MCF-7	breast:
13	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
14	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
15	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
16	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
17	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
18	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
19	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
20	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
21	chr2:133427399..133430167-chr2:133804238..133806785,2	MCF-7	breast:
22	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
23	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
24	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
25	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-12	chr2:133740284-133740478	ucscGeneNc_uc002ttu_1
2	lnc-GPR39-12	chr2:133742958-133743083	ucscGeneNc_uc002ttu_1
3	lnc-GPR39-12	chr2:133742398-133742484	ucscGeneNc_uc002ttu_1
4	lnc-GPR39-12	chr2:133741315-133741466	ucscGeneNc_uc002ttu_1

No data

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000150551	chromatin interactions

Extended variants
information (count: 6602 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:6602 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549344660	chr2:133722681-133722682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566910410	chr2:133722783-133722784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13417008	chr2:133722787-133722788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs58125250	chr2:133722898-133722899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs550678819	chr2:133722905-133722906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567502356	chr2:133723121-133723122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189450571	chr2:133723134-133723135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556809743	chr2:133723137-133723138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112035764	chr2:133723157-133723158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571192765	chr2:133723160-133723161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182005230	chr2:133723187-133723188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145661115	chr2:133723193-133723194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553608791	chr2:133723243-133723244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572077005	chr2:133723395-133723396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542731108	chr2:133723396-133723397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185251529	chr2:133723400-133723401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576301214	chr2:133723424-133723425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114012544	chr2:133723437-133723438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565147975	chr2:133723443-133723444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189036466	chr2:133723451-133723452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564718652	chr2:133723477-133723478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372938681	chr2:133723478-133723479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180990983	chr2:133723479-133723480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550361232	chr2:133723515-133723516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60589235	chr2:133723516-133723517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562355593	chr2:133723570-133723571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369684736	chr2:133723576-133723577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147730092	chr2:133723578-133723579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139892007	chr2:133723626-133723627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553239480	chr2:133723633-133723634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59633875	chr2:133723658-133723659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs149812973	chr2:133723681-133723682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550214534	chr2:133723704-133723705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565641949	chr2:133723705-133723706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549870313	chr2:133723717-133723718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571884391	chr2:133723735-133723736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538272277	chr2:133723736-133723737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553767891	chr2:133723786-133723787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375553381	chr2:133723833-133723834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565660904	chr2:133723921-133723922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536399991	chr2:133723931-133723932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554696689	chr2:133723964-133723965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145773196	chr2:133723978-133723979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538856953	chr2:133724023-133724024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536424524	chr2:133724027-133724028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537195769	chr2:133724047-133724048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558599058	chr2:133724048-133724049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577032950	chr2:133724078-133724079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540952075	chr2:133724119-133724120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560560357	chr2:133724120-133724121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133701600-133727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:133702200-133724400	Weak transcription	Brain Hippocampus Middle	brain
3	chr2:133714600-133735400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:133718600-133727000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:133720200-133724000	Weak transcription	Liver	Liver
6	chr2:133721400-133732200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:133722400-133724200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:133724200-133724800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:133724400-133725800	Enhancers	Brain Hippocampus Middle	brain
10	chr2:133724800-133725400	Weak transcription	Brain Anterior Caudate	brain
11	chr2:133724800-133725800	Enhancers	Brain Substantia Nigra	brain
12	chr2:133724800-133728200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:133725400-133725600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:133725400-133725600	Enhancers	Brain Anterior Caudate	brain
15	chr2:133725400-133725800	Enhancers	Brain Angular Gyrus	brain
16	chr2:133725400-133725800	Enhancers	Brain Cingulate Gyrus	brain
17	chr2:133725600-133726200	Weak transcription	Brain Anterior Caudate	brain
18	chr2:133725800-133727200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:133725800-133732600	Weak transcription	Brain Hippocampus Middle	brain
20	chr2:133726200-133726400	Enhancers	Brain Anterior Caudate	brain
21	chr2:133726400-133734800	Weak transcription	Brain Anterior Caudate	brain
22	chr2:133726600-133727600	Enhancers	HUVEC	blood vessel
23	chr2:133726800-133727400	Enhancers	NHEK	skin
24	chr2:133727000-133727400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:133727000-133727400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:133727000-133727400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:133727000-133727400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:133727200-133727400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:133727200-133727400	Enhancers	Esophagus	oesophagus
30	chr2:133727400-133728000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:133727400-133728400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:133727400-133728800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:133727400-133729200	Weak transcription	NHEK	skin
34	chr2:133727400-133732000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:133728200-133729400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:133728400-133729000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:133728400-133730200	Enhancers	Stomach Mucosa	stomach
38	chr2:133728800-133730000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:133729200-133730000	Enhancers	NHEK	skin
40	chr2:133729400-133730000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:133729400-133733000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:133730000-133732200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:133730000-133732200	Weak transcription	NHEK	skin
44	chr2:133730000-133735400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:133731800-133732400	Enhancers	Colon Smooth Muscle	Colon
46	chr2:133732000-133732600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:133732000-133732600	Enhancers	Fetal Stomach	stomach
48	chr2:133732000-133733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr2:133732000-133733400	Enhancers	Fetal Kidney	kidney
50	chr2:133732000-133733600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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