Variant report

Variant	nsv875260
Chromosome Location	chr2:144675354-144703126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:187)
CpG islands
(count:551)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:187 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:144694319-144694938	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr2:144700446-144700541	K562	blood:	n/a	n/a
3	BHLHE40	chr2:144694421-144694903	GM12878	blood:	n/a	n/a
4	CBX3	chr2:144676107-144676453	K562	blood:	n/a	n/a
5	CBX3	chr2:144676114-144676441	K562	blood:	n/a	n/a
6	CBX3	chr2:144678934-144679199	K562	blood:	n/a	n/a
7	CCNT2	chr2:144694551-144694978	K562	blood:	n/a	n/a
8	CEBPB	chr2:144688558-144688597	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:144689657-144689777	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:144684363-144684690	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:144693909-144694106	A549	lung:	n/a	chr2:144694036-144694049 chr2:144694036-144694049 chr2:144694036-144694049
12	CEBPB	chr2:144687213-144687497	IMR90	lung:	n/a	chr2:144687388-144687399
13	CEBPB	chr2:144693917-144694117	H1-hESC	embryonic stem cell:	n/a	chr2:144694036-144694049 chr2:144694036-144694049 chr2:144694036-144694049
14	CEBPB	chr2:144687247-144687560	HepG2	liver:	n/a	chr2:144687388-144687399
15	CHD1	chr2:144694853-144695595	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr2:144695013-144695210	GM12878	blood:	n/a	n/a
17	CHD2	chr2:144698325-144698360	GM12878	blood:	n/a	n/a
18	CHD2	chr2:144694795-144694925	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr2:144694692-144695174	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr2:144694650-144695315	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr2:144694298-144695489	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:144687440-144687590	GM12873	blood:	n/a	n/a
23	CTCF	chr2:144687460-144687610	GM12865	blood:	n/a	n/a
24	CTCF	chr2:144687360-144687510	GM12873	blood:	n/a	n/a
25	CTCF	chr2:144687495-144687650	K562	blood:	n/a	n/a
26	CTCF	chr2:144694860-144694987	ProgFib	skin:	n/a	n/a
27	CTCF	chr2:144687500-144687650	GM12872	blood:	n/a	n/a
28	CTCF	chr2:144703080-144703230	AG10803	skin:	n/a	n/a
29	CTCF	chr2:144687480-144687630	GM12878	blood:	n/a	n/a
30	CTCF	chr2:144687505-144687635	GM19239	blood:	n/a	n/a
31	CTCF	chr2:144694820-144694970	AG04449	skin:	n/a	n/a
32	CTCF	chr2:144694894-144695005	GM12892	blood:	n/a	n/a
33	CTCF	chr2:144694885-144694973	GM19240	blood:	n/a	n/a
34	CTCF	chr2:144694720-144694870	GM12873	blood:	n/a	n/a
35	CTCF	chr2:144694916-144695009	GM19238	blood:	n/a	n/a
36	CTCF	chr2:144687500-144687650	HMF	breast:	n/a	n/a
37	CTCF	chr2:144694722-144694788	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:144694887-144694975	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:144687520-144687670	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr2:144687553-144687580	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:144687549-144687576	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr2:144687421-144687733	GM12878	blood:	n/a	n/a
43	CTCF	chr2:144694743-144695042	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:144687520-144687593	GM13976	blood:	n/a	n/a
45	CTCF	chr2:144687572-144687607	HepG2	liver:	n/a	n/a
46	CTCF	chr2:144687557-144687580	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:144687521-144687594	GM10266	blood:	n/a	n/a
48	CTCF	chr2:144694927-144694992	Gliobla	brain:	n/a	n/a
49	CTCF	chr2:144687540-144687690	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr2:144687544-144687616	NHEK	skin:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:144695078-144695128	AG04450	lung:	fetal
2	chr2:144695179-144695229	K562	blood:	n/a
3	chr2:144695078-144695128	AG04450	lung:	fetal
4	chr2:144695179-144695229	K562	blood:	n/a
5	chr2:144695257-144695307	IMR90	lung:	fetal
6	chr2:144694680-144694730	HRCEpiC	kidney:	n/a
7	chr2:144694405-144694455	PANC-1	pancreas:	n/a
8	chr2:144694680-144694730	NH-A	brain:	n/a
9	chr2:144695179-144695229	CMK	blood:	n/a
10	chr2:144695257-144695307	AoSMC	blood vessel:	n/a
11	chr2:144693693-144693743	AG09319	gingival:	n/a
12	chr2:144695257-144695307	CMK	blood:	n/a
13	chr2:144695078-144695128	GM12878	blood:	n/a
14	chr2:144694809-144694859	HCT-116	colon:	n/a
15	chr2:144698389-144698439	GM19239	blood:	n/a
16	chr2:144693693-144693743	HEEpiC	esophagus:	n/a
17	chr2:144695179-144695229	NB4	blood:	n/a
18	chr2:144698389-144698439	BE2_C	brain:	n/a
19	chr2:144692640-144692690	GM06990	blood:	n/a
20	chr2:144695078-144695128	PFSK-1	brain:	n/a
21	chr2:144695257-144695307	NT2-D1	testis:	n/a
22	chr2:144698389-144698439	HCT-116	colon:	n/a
23	chr2:144693693-144693743	HRCEpiC	kidney:	n/a
24	chr2:144694680-144694730	SK-N-MC	brain:	n/a
25	chr2:144695257-144695307	GM12892	blood:	n/a
26	chr2:144692640-144692690	ECC-1	luminal epithelium:	n/a
27	chr2:144693693-144693743	HNPCEpiC	eye:	n/a
28	chr2:144692640-144692690	HEEpiC	esophagus:	n/a
29	chr2:144698389-144698439	AG09319	gingival:	n/a
30	chr2:144693693-144693743	T-47D	breast:	n/a
31	chr2:144698389-144698439	HRCEpiC	kidney:	n/a
32	chr2:144698389-144698439	PANC-1	pancreas:	n/a
33	chr2:144692640-144692690	SK-N-MC	brain:	n/a
34	chr2:144694809-144694859	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:144698389-144698439	NT2-D1	testis:	n/a
36	chr2:144692640-144692690	AoSMC	blood vessel:	n/a
37	chr2:144695257-144695307	Hela-S3	cervix:	n/a
38	chr2:144692640-144692690	HCT-116	colon:	n/a
39	chr2:144695257-144695307	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:144694405-144694455	HNPCEpiC	eye:	n/a
41	chr2:144695257-144695307	PrEC	prostate:	n/a
42	chr2:144695078-144695128	HepG2	liver:	n/a
43	chr2:144695078-144695128	H1-hESC	embryonic stem cell:	embryo
44	chr2:144695257-144695307	AG10803	skin:	n/a
45	chr2:144693693-144693743	NHBE	bronchial:	n/a
46	chr2:144698389-144698439	HNPCEpiC	eye:	n/a
47	chr2:144694405-144694455	H1-hESC	embryonic stem cell:	embryo
48	chr2:144694680-144694730	HEK293	kidney:	embryo
49	chr2:144694680-144694730	HNPCEpiC	eye:	n/a
50	chr2:144694680-144694730	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:144681574..144683750-chr2:144691363..144693322,2	K562	blood:
2	chr2:144687027..144688572-chr2:144690618..144693270,2	K562	blood:
3	chr2:144681574..144683750-chr2:144691363..144693322,2	K562	blood:
4	chr2:144700229..144702979-chr2:145088047..145090222,2	MCF-7	breast:
5	chr2:144697765..144699477-chr2:144704589..144707324,2	K562	blood:
6	chr2:144669898..144672819-chr2:144685231..144687697,2	K562	blood:
7	chr2:144697977..144700307-chr2:144703407..144706089,2	K562	blood:
8	chr2:144684000..144686293-chr2:145089370..145091647,2	K562	blood:
9	chr2:144687027..144688572-chr2:144690618..144693270,2	K562	blood:
10	chr2:144685234..144688030-chr2:144717125..144719002,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP15-2	chr2:144698693-144698731	NONHSAT074752
2	lnc-GTDC1-8	chr2:144695635-144696173	NONHSAT074751
3	lnc-ARHGAP15-2	chr2:144694640-144695203	ENSG00000232377.1
4	lnc-ARHGAP15-2	chr2:144698581-144698731	NR_110237
5	lnc-ARHGAP15-2	chr2:144694634-144695203	NR_110237
6	lnc-ARHGAP15-2	chr2:144698581-144698731	ENSG00000232377.1

No data

Variant related genes	Relation type
ENSG00000232377	TF binding region
ENSG00000232377	CpG island
ENSG00000121964	chromatin interactions
G3BP2	miRNA target sites

Extended variants
information (count: 941 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs787143	chr2:144675354-144675355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189514744	chr2:144675378-144675379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144816274	chr2:144675411-144675412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556204403	chr2:144675460-144675461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551973886	chr2:144675499-144675500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs80304908	chr2:144675619-144675620	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs375590991	chr2:144675638-144675639	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs111245520	chr2:144675651-144675652	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs373634775	chr2:144675652-144675653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs193172325	chr2:144675653-144675654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs35094283	chr2:144675668-144675669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs545617238	chr2:144675673-144675674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs563893163	chr2:144675690-144675691	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs570577877	chr2:144675726-144675727	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs549855955	chr2:144675727-144675728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs370543544	chr2:144675755-144675756	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs529262252	chr2:144675790-144675791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs547807257	chr2:144675882-144675883	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs185068594	chr2:144675943-144675944	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs537670372	chr2:144675944-144675945	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs144361620	chr2:144675945-144675946	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs189347996	chr2:144675973-144675974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs558386289	chr2:144675992-144675993	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs787142	chr2:144675994-144675995	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs181749131	chr2:144676105-144676106	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs375309695	chr2:144676108-144676109	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs556273280	chr2:144676154-144676155	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs567455321	chr2:144676164-144676165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs541826883	chr2:144676221-144676222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs184671432	chr2:144676273-144676274	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs572310223	chr2:144676294-144676295	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs531502787	chr2:144676299-144676300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs553030941	chr2:144676365-144676366	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs138651908	chr2:144676414-144676415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs371167520	chr2:144676485-144676486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs188340699	chr2:144676492-144676493	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs141494321	chr2:144676541-144676542	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs529332710	chr2:144676569-144676570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs77103320	chr2:144676609-144676610	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs75718412	chr2:144676618-144676619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs531426961	chr2:144676733-144676734	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs547791333	chr2:144676791-144676792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs77764578	chr2:144676816-144676817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377732251	chr2:144676856-144676857	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180766921	chr2:144676857-144676858	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570291606	chr2:144676885-144676886	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186615753	chr2:144677063-144677064	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191064243	chr2:144677150-144677151	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117320818	chr2:144677157-144677158	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535429484	chr2:144677292-144677293	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	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	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	20456320	CNVD
Hirschsprung''s Disease	21712996	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144674000-144675600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:144674200-144675600	Weak transcription	Fetal Lung	lung
3	chr2:144675600-144676000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:144675600-144676800	ZNF genes & repeats	Fetal Lung	lung
5	chr2:144675800-144676200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:144676200-144677600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:144676800-144690600	Weak transcription	Fetal Lung	lung
8	chr2:144677800-144678400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:144678400-144685600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:144682200-144685600	Weak transcription	Fetal Kidney	kidney
11	chr2:144683000-144683200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:144683200-144683400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:144683400-144684400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:144683400-144685200	Enhancers	Fetal Intestine Large	intestine
15	chr2:144683600-144684000	Enhancers	K562	blood
16	chr2:144683600-144684400	Enhancers	Fetal Intestine Small	intestine
17	chr2:144683800-144684400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:144683800-144684400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr2:144684400-144685600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:144685600-144685800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr2:144685600-144686600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:144685600-144686600	Enhancers	Fetal Kidney	kidney
23	chr2:144685600-144686600	Enhancers	Ovary	ovary
24	chr2:144685600-144686800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:144685800-144686200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:144685800-144686200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
27	chr2:144685800-144686600	Enhancers	HSMM	muscle
28	chr2:144686000-144686600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:144686200-144691600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:144686400-144686600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr2:144686400-144686800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:144686600-144687000	Weak transcription	HSMM	muscle
33	chr2:144686600-144689600	Weak transcription	Fetal Kidney	kidney
34	chr2:144686600-144691200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:144686600-144692400	Weak transcription	Ovary	ovary
36	chr2:144686800-144690600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:144686800-144691000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:144689600-144694000	Enhancers	Fetal Kidney	kidney
39	chr2:144689800-144690000	Enhancers	Fetal Stomach	stomach
40	chr2:144690000-144691800	Weak transcription	Fetal Stomach	stomach
41	chr2:144690600-144692000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:144690600-144692000	Enhancers	Fetal Lung	lung
43	chr2:144691000-144691400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:144691000-144692800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:144691200-144693600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:144691200-144694000	Weak transcription	HSMM	muscle
47	chr2:144691200-144694200	Enhancers	Fetal Intestine Large	intestine
48	chr2:144691200-144694200	Enhancers	Fetal Intestine Small	intestine
49	chr2:144691400-144691600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:144691400-144692200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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