Variant report

Variant	nsv2931
Chromosome Location	chr2:133625818-133670963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:133653618-133653917	GM12878	blood:	n/a	n/a
2	CEBPB	chr2:133641884-133642228	A549	lung:	n/a	chr2:133642044-133642055
3	CEBPB	chr2:133641936-133642152	A549	lung:	n/a	chr2:133642044-133642055
4	CEBPB	chr2:133667172-133667379	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:133665111-133665208	HepG2	liver:	n/a	chr2:133665148-133665159
6	CEBPB	chr2:133659336-133659561	HepG2	liver:	n/a	chr2:133659455-133659466
7	CEBPB	chr2:133641988-133642086	HepG2	liver:	n/a	chr2:133642044-133642055
8	CEBPB	chr2:133641865-133642307	A549	lung:	n/a	chr2:133642044-133642055
9	CTCF	chr2:133669700-133669850	GM12872	blood:	n/a	n/a
10	CTCF	chr2:133669620-133669770	RPTEC	kidney:	n/a	n/a
11	CTCF	chr2:133669651-133669851	Fibrobl	skin:	n/a	n/a
12	CTCF	chr2:133669680-133669830	AG04449	skin:	n/a	n/a
13	CTCF	chr2:133669680-133669830	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr2:133669620-133669770	HVMF	connective:	n/a	n/a
15	CTCF	chr2:133669640-133669790	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr2:133669743-133669772	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr2:133669628-133669838	HepG2	liver:	n/a	n/a
18	CTCF	chr2:133660400-133660550	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr2:133669678-133669834	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:133669640-133669790	HMEC	breast:	n/a	n/a
21	CTCF	chr2:133669578-133669848	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:133669720-133669870	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr2:133669683-133669771	GM19240	blood:	n/a	n/a
24	CTCF	chr2:133647460-133647610	Caco-2	colon:	n/a	n/a
25	CTCF	chr2:133669660-133669810	Caco-2	colon:	n/a	n/a
26	CTCF	chr2:133669700-133669850	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr2:133669676-133669834	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:133669680-133669830	NHEK	skin:	n/a	n/a
29	CTCF	chr2:133632875-133633007	H1-hESC	embryonic stem cell:	n/a	chr2:133632945-133632966 chr2:133632950-133632968 chr2:133632953-133632963
30	CTCF	chr2:133669710-133669800	Medullo	brain:	n/a	n/a
31	CTCF	chr2:133669620-133669770	HPF	lung:	n/a	n/a
32	CTCF	chr2:133669620-133669770	HepG2	liver:	n/a	n/a
33	CTCF	chr2:133669670-133669820	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr2:133669700-133669850	BE2_C	brain:	n/a	n/a
35	CTCF	chr2:133632923-133633014	MCF-7	breast:	n/a	chr2:133632945-133632966 chr2:133632950-133632968 chr2:133632953-133632963
36	CTCF	chr2:133669660-133669810	AG04449	skin:	n/a	n/a
37	CTCF	chr2:133669740-133669890	AG04450	lung:	n/a	n/a
38	CTCF	chr2:133669340-133669490	HCM	heart:	n/a	n/a
39	CTCF	chr2:133669780-133669930	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:133669651-133669855	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:133669640-133669790	BJ	skin:	n/a	n/a
42	CTCF	chr2:133669700-133669850	AG09319	gingival:	n/a	n/a
43	CTCF	chr2:133669680-133669830	Caco-2	colon:	n/a	n/a
44	CTCF	chr2:133669740-133669890	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:133669633-133669870	IMR90	lung:	n/a	n/a
46	CTCF	chr2:133669700-133669850	HEK293	kidney:	n/a	n/a
47	CTCF	chr2:133632800-133632950	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:133669686-133669786	GM19239	blood:	n/a	n/a
49	CTCF	chr2:133669660-133669810	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:133669660-133669810	HA-sp	spinal cord:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133635152-133635202	PFSK-1	brain:	n/a
2	chr2:133635152-133635202	ECC-1	luminal epithelium:	n/a
3	chr2:133670347-133670397	NH-A	brain:	n/a
4	chr2:133670347-133670397	ovcar-3	ovarian:	n/a
5	chr2:133635152-133635202	HCM	heart:	n/a
6	chr2:133670347-133670397	NHDF-neo	bronchial:	n/a
7	chr2:133670347-133670397	NB4	blood:	n/a
8	chr2:133670347-133670397	HEK293	kidney:	embryo
9	chr2:133670347-133670397	HRE	kidney:	n/a
10	chr2:133670347-133670397	HIPEpiC	eye:	n/a
11	chr2:133670347-133670397	AG09319	gingival:	n/a
12	chr2:133630172-133630222	HCM	heart:	n/a
13	chr2:133630172-133630222	HRPEpiC	eye:	n/a
14	chr2:133670347-133670397	PrEC	prostate:	n/a
15	chr2:133670347-133670397	HNPCEpiC	eye:	n/a
16	chr2:133630172-133630222	A549	lung:	n/a
17	chr2:133635152-133635202	Hela-S3	cervix:	n/a
18	chr2:133635152-133635202	HRE	kidney:	n/a
19	chr2:133635152-133635202	Hepatocyte	liver:	n/a
20	chr2:133670347-133670397	SK-N-SH_RA	brain:	n/a
21	chr2:133670347-133670397	PFSK-1	brain:	n/a
22	chr2:133670347-133670397	HRPEpiC	eye:	n/a
23	chr2:133670347-133670397	GM12878	blood:	n/a
24	chr2:133635152-133635202	GM12878	blood:	n/a
25	chr2:133630172-133630222	ProgFib	skin:	n/a
26	chr2:133630172-133630222	T-47D	breast:	n/a
27	chr2:133630172-133630222	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:133630172-133630222	MCF10A-Er-Src	breast:	n/a
29	chr2:133630172-133630222	SAEC	small airway:	n/a
30	chr2:133630172-133630222	SK-N-MC	brain:	n/a
31	chr2:133630172-133630222	HNPCEpiC	eye:	n/a
32	chr2:133635152-133635202	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:133635152-133635202	HepG2	liver:	n/a
34	chr2:133630172-133630222	HEEpiC	esophagus:	n/a
35	chr2:133630172-133630222	HRE	kidney:	n/a
36	chr2:133630172-133630222	GM12878	blood:	n/a
37	chr2:133635152-133635202	GM06990	blood:	n/a
38	chr2:133630172-133630222	SK-N-SH_RA	brain:	n/a
39	chr2:133630172-133630222	NT2-D1	testis:	n/a
40	chr2:133630172-133630222	GM12892	blood:	n/a
41	chr2:133630172-133630222	SK-N-SH	brain:	n/a
42	chr2:133635152-133635202	ovcar-3	ovarian:	n/a
43	chr2:133635152-133635202	HCPEpiC	choroid plexus:	n/a
44	chr2:133635152-133635202	HMEC	breast:	n/a
45	chr2:133630172-133630222	AG10803	skin:	n/a
46	chr2:133630172-133630222	ovcar-3	ovarian:	n/a
47	chr2:133630172-133630222	NHDF-neo	bronchial:	n/a
48	chr2:133670347-133670397	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:133635152-133635202	SK-N-SH	brain:	n/a
50	chr2:133635152-133635202	BE2_C	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
2	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
3	chr2:133422076..133424197-chr2:133633337..133635605,2	MCF-7	breast:
4	chr2:133339779..133340732-chr2:133641136..133642087,4	MCF-7	breast:
5	chr2:133339765..133340550-chr2:133641463..133642066,3	MCF-7	breast:
6	chr2:133339874..133340573-chr2:133634427..133634936,2	MCF-7	breast:
7	chr2:133632988..133635026-chr2:133635332..133637813,2	MCF-7	breast:
8	chr2:133632988..133635026-chr2:133635332..133637813,2	MCF-7	breast:
9	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
10	chr2:133607951..133610816-chr2:133632079..133634420,2	MCF-7	breast:
11	chr2:133339874..133340573-chr2:133634427..133635308,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000228721	TF binding region
ENSG00000233729	TF binding region
ENSG00000228721	CpG island
ENSG00000233729	CpG island

Extended variants
information (count: 1759 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1759 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72847276	chr2:133625822-133625823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189156238	chr2:133625878-133625879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74532358	chr2:133625901-133625902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561731181	chr2:133625948-133625949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563984400	chr2:133625958-133625959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531071343	chr2:133625978-133625979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140798876	chr2:133626051-133626052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112998697	chr2:133626067-133626068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369275489	chr2:133626083-133626084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544651507	chr2:133626091-133626092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115881268	chr2:133626106-133626107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544297351	chr2:133626134-133626135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13389841	chr2:133626142-133626143	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs16842771	chr2:133626155-133626156	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs558007661	chr2:133626158-133626159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192546724	chr2:133626184-133626185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371003159	chr2:133626223-133626224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76935750	chr2:133626250-133626251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144672164	chr2:133626259-133626260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183593385	chr2:133626351-133626352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138540981	chr2:133626381-133626382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188338311	chr2:133626449-133626450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551639601	chr2:133626460-133626461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201785070	chr2:133626513-133626514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141515246	chr2:133626515-133626516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373650440	chr2:133626527-133626528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559905727	chr2:133626536-133626537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376932881	chr2:133626539-133626540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574949106	chr2:133626560-133626561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542452278	chr2:133626569-133626570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371150795	chr2:133626590-133626591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145207101	chr2:133626596-133626597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115812874	chr2:133626609-133626610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181220304	chr2:133626613-133626614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528097025	chr2:133626619-133626620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139029192	chr2:133626621-133626622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543629222	chr2:133626628-133626629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567823918	chr2:133626631-133626632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527941646	chr2:133626684-133626685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs17326258	chr2:133626706-133626707	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550260290	chr2:133626716-133626717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568038574	chr2:133626805-133626806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80110233	chr2:133626827-133626828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117873087	chr2:133626902-133626903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16842790	chr2:133626910-133626911	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs186498645	chr2:133626926-133626927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114679759	chr2:133626982-133626983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12466020	chr2:133626988-133626989	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs139765559	chr2:133626990-133626991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189928768	chr2:133627009-133627010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133592200-133634000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133606400-133635200	Weak transcription	Ovary	ovary
3	chr2:133613800-133629400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:133615200-133629400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:133618200-133635400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:133621000-133645200	Weak transcription	Left Ventricle	heart
7	chr2:133621600-133628200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:133622200-133628600	Weak transcription	Fetal Lung	lung
9	chr2:133628200-133630400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:133628600-133630400	Enhancers	Fetal Lung	lung
11	chr2:133629200-133630400	Enhancers	Fetal Heart	heart
12	chr2:133629400-133629800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:133629400-133630000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:133629400-133630200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:133629400-133630600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:133629600-133630000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:133629600-133630000	Enhancers	Brain Hippocampus Middle	brain
18	chr2:133629600-133630200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:133629600-133630200	Enhancers	Lung	lung
20	chr2:133629600-133630200	Enhancers	Right Ventricle	heart
21	chr2:133629600-133630600	Enhancers	Fetal Muscle Leg	muscle
22	chr2:133629600-133631000	Enhancers	Fetal Muscle Trunk	muscle
23	chr2:133629800-133630600	Enhancers	Right Atrium	heart
24	chr2:133630000-133630600	Enhancers	Placenta	Placenta
25	chr2:133630000-133632800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:133630000-133632800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:133630000-133635200	Weak transcription	Brain Hippocampus Middle	brain
28	chr2:133630200-133635000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:133630200-133643400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:133630400-133638800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:133630600-133631000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:133631600-133634200	Weak transcription	Hela-S3	cervix
33	chr2:133632000-133632800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:133632200-133632600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:133632600-133633000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr2:133632800-133633000	Enhancers	H9 Cell Line	embryonic stem cell
37	chr2:133632800-133633200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr2:133632800-133633200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:133632800-133633800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:133633400-133633800	Enhancers	NHLF	lung
41	chr2:133633800-133634200	Weak transcription	NHLF	lung
42	chr2:133633800-133634600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:133633800-133636800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:133634200-133635000	Enhancers	NHLF	lung
45	chr2:133634200-133635200	Enhancers	Hela-S3	cervix
46	chr2:133634600-133635400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:133635000-133635200	Enhancers	Gastric	stomach
48	chr2:133635000-133635600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:133635000-133637200	Weak transcription	NHLF	lung
50	chr2:133635200-133636000	Strong transcription	Brain Hippocampus Middle	brain

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