Variant report

Variant	nsv1003983
Chromosome Location	chr2:178551958-178577002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:281)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178556633-178557685	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:178554400-178554623	K562	blood:	n/a	n/a
3	ARID3A	chr2:178558288-178559366	K562	blood:	n/a	n/a
4	ARID3A	chr2:178557491-178557668	K562	blood:	n/a	n/a
5	ATF1	chr2:178554407-178554764	K562	blood:	n/a	n/a
6	ATF1	chr2:178558560-178559091	K562	blood:	n/a	n/a
7	ATF3	chr2:178558359-178559087	K562	blood:	n/a	n/a
8	BHLHE40	chr2:178557739-178557741	K562	blood:	n/a	n/a
9	BHLHE40	chr2:178558039-178559104	K562	blood:	n/a	n/a
10	BHLHE40	chr2:178554454-178554631	K562	blood:	n/a	n/a
11	CCNT2	chr2:178558442-178559135	K562	blood:	n/a	chr2:178558864-178558884
12	CCNT2	chr2:178554360-178554689	K562	blood:	n/a	n/a
13	CEBPB	chr2:178557240-178557599	HepG2	liver:	n/a	chr2:178557583-178557595
14	CEBPB	chr2:178558415-178558716	HepG2	liver:	n/a	chr2:178558576-178558587
15	CEBPB	chr2:178558569-178558614	H1-hESC	embryonic stem cell:	n/a	chr2:178558576-178558587
16	CEBPB	chr2:178558315-178559143	K562	blood:	n/a	chr2:178558576-178558587
17	CEBPB	chr2:178557275-178557602	A549	lung:	n/a	chr2:178557583-178557595
18	CEBPB	chr2:178558399-178559087	K562	blood:	n/a	chr2:178558576-178558587
19	CEBPB	chr2:178557191-178557717	A549	lung:	n/a	chr2:178557583-178557595
20	CEBPB	chr2:178558429-178558729	A549	lung:	n/a	chr2:178558576-178558587
21	CEBPB	chr2:178557263-178557501	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:178558425-178559027	K562	blood:	n/a	chr2:178558576-178558587
23	CEBPB	chr2:178557271-178557521	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:178558416-178558685	IMR90	lung:	n/a	chr2:178558576-178558587
25	CEBPB	chr2:178569543-178569609	HepG2	liver:	n/a	chr2:178569565-178569576
26	CEBPD	chr2:178558470-178559144	K562	blood:	n/a	n/a
27	CEBPD	chr2:178558362-178559103	K562	blood:	n/a	n/a
28	CTCF	chr2:178555980-178556130	NHEK	skin:	n/a	chr2:178555992-178556001
29	CTCF	chr2:178557580-178557730	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr2:178557640-178557790	HFF	foreskin:	n/a	n/a
31	CTCF	chr2:178557640-178557790	A549	lung:	n/a	n/a
32	CTCF	chr2:178557640-178557790	NHEK	skin:	n/a	n/a
33	CTCF	chr2:178555960-178556110	GM12872	blood:	n/a	chr2:178555992-178556001
34	CTCF	chr2:178557680-178557830	NHEK	skin:	n/a	n/a
35	CTCF	chr2:178557680-178557830	HMEC	breast:	n/a	n/a
36	CTCF	chr2:178556080-178556230	NHEK	skin:	n/a	n/a
37	CTCF	chr2:178557700-178557850	RPTEC	kidney:	n/a	n/a
38	CTCF	chr2:178557640-178557790	SAEC	small airway:	n/a	n/a
39	CTCF	chr2:178556040-178556190	HRE	kidney:	n/a	n/a
40	CTCF	chr2:178556040-178556190	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr2:178557680-178557830	AG09319	gingival:	n/a	n/a
42	CTCF	chr2:178557600-178557750	HEK293	kidney:	n/a	n/a
43	CTCF	chr2:178557686-178557763	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:178557610-178557815	A549	lung:	n/a	n/a
45	CTCF	chr2:178556020-178556170	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:178556040-178556190	GM12865	blood:	n/a	n/a
47	CTCF	chr2:178557640-178557790	HMEC	breast:	n/a	n/a
48	CTCF	chr2:178557598-178557886	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:178557640-178557790	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:178557700-178557850	HRPEpiC	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178556488-178556538	NH-A	brain:	n/a
2	chr2:178556488-178556538	NB4	blood:	n/a
3	chr2:178556488-178556538	PFSK-1	brain:	n/a
4	chr2:178556488-178556538	PANC-1	pancreas:	n/a
5	chr2:178556488-178556538	GM12891	blood:	n/a
6	chr2:178556488-178556538	HCF	heart:	n/a
7	chr2:178556488-178556538	BE2_C	brain:	n/a
8	chr2:178556488-178556538	SKMC	muscle:	n/a
9	chr2:178556488-178556538	NT2-D1	testis:	n/a
10	chr2:178556488-178556538	MCF-7	breast:	n/a
11	chr2:178556488-178556538	A549	lung:	n/a
12	chr2:178556488-178556538	Caco-2	colon:	n/a
13	chr2:178556488-178556538	BJ	skin:	n/a
14	chr2:178556488-178556538	NHDF-neo	bronchial:	n/a
15	chr2:178556488-178556538	HRPEpiC	eye:	n/a
16	chr2:178556488-178556538	AG09309	skin:	n/a
17	chr2:178556488-178556538	HCPEpiC	choroid plexus:	n/a
18	chr2:178556488-178556538	HUVEC	blood vessel:	n/a
19	chr2:178556488-178556538	RPTEC	kidney:	n/a
20	chr2:178556488-178556538	SK-N-MC	brain:	n/a
21	chr2:178556488-178556538	HEK293	kidney:	embryo
22	chr2:178556488-178556538	IMR90	lung:	fetal
23	chr2:178556488-178556538	SK-N-SH	brain:	n/a
24	chr2:178556488-178556538	H1-hESC	embryonic stem cell:	embryo
25	chr2:178556488-178556538	HMEC	breast:	n/a
26	chr2:178556488-178556538	Hela-S3	cervix:	n/a
27	chr2:178556488-178556538	HL-60	blood:	n/a
28	chr2:178556488-178556538	ProgFib	skin:	n/a
29	chr2:178556488-178556538	HNPCEpiC	eye:	n/a
30	chr2:178556488-178556538	HRCEpiC	kidney:	n/a
31	chr2:178556488-178556538	HIPEpiC	eye:	n/a
32	chr2:178556488-178556538	GM12878	blood:	n/a
33	chr2:178556488-178556538	HAEpiC	amniotic membrane:	n/a
34	chr2:178556488-178556538	HCT-116	colon:	n/a
35	chr2:178556488-178556538	ovcar-3	ovarian:	n/a
36	chr2:178556488-178556538	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:178556488-178556538	LNCaP	prostate:	n/a
38	chr2:178556488-178556538	HEEpiC	esophagus:	n/a
39	chr2:178556488-178556538	PrEC	prostate:	n/a
40	chr2:178556488-178556538	SK-N-SH_RA	brain:	n/a
41	chr2:178556488-178556538	HRE	kidney:	n/a
42	chr2:178556488-178556538	T-47D	breast:	n/a
43	chr2:178556488-178556538	ECC-1	luminal epithelium:	n/a
44	chr2:178556488-178556538	GM06990	blood:	n/a
45	chr2:178556488-178556538	AG09319	gingival:	n/a
46	chr2:178556488-178556538	AG04450	lung:	fetal
47	chr2:178556488-178556538	AG10803	skin:	n/a
48	chr2:178556488-178556538	AG04449	skin:	fetal
49	chr2:178556488-178556538	MCF10A-Er-Src	breast:	n/a
50	chr2:178556488-178556538	HCM	heart:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
2	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
3	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:
4	chr2:178553724..178556122-chr2:178557669..178561053,4	K562	blood:
5	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
6	chr2:178557613..178559704-chr2:178561778..178563487,2	K562	blood:
7	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
8	chr2:178546208..178548509-chr2:178552748..178555951,3	K562	blood:
9	chr2:178573812..178575590-chr2:178578150..178581099,2	K562	blood:
10	chr2:178257363..178259725-chr2:178564767..178567324,2	K562	blood:
11	chr2:178556581..178559111-chr2:178571009..178573713,2	K562	blood:
12	chr2:178416053..178418708-chr2:178570239..178572777,3	MCF-7	breast:
13	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
14	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
15	chr2:178561119..178564111-chr2:178566483..178568629,4	K562	blood:
16	chr2:178560703..178563309-chr2:178574867..178577003,2	K562	blood:
17	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
18	chr2:178557827..178560384-chr2:178566181..178567818,2	K562	blood:
19	chr2:178563706..178566606-chr2:178575234..178578088,2	K562	blood:
20	chr2:178561612..178563811-chr2:178565917..178568583,4	K562	blood:
21	chr2:178562301..178565158-chr2:178568749..178571184,2	K562	blood:
22	chr2:178536377..178538004-chr2:178556463..178558808,2	K562	blood:
23	chr2:178554622..178556769-chr2:178559553..178561777,2	K562	blood:
24	chr2:178559293..178562880-chr2:178620510..178622541,4	K562	blood:
25	chr2:178562301..178564741-chr2:178568694..178570249,2	K562	blood:
26	chr2:178454525..178456445-chr2:178573217..178575511,2	K562	blood:
27	chr2:178570926..178572812-chr2:178573756..178576490,2	K562	blood:
28	chr2:178561207..178563093-chr2:178570078..178571660,2	MCF-7	breast:
29	chr2:178568725..178571101-chr2:178581270..178584257,2	K562	blood:
30	chr2:178567581..178570235-chr2:178573899..178577717,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPS-3	chr2:178563218-178563299	ENSG00000229941.1
2	lnc-AGPS-3	chr2:178565822-178565956	ENSG00000229941.1
3	lnc-AGPS-3	chr2:178567216-178567477	ENSG00000229941.1
4	lnc-AGPS-3	chr2:178563157-178563299	ENSG00000229941.1
5	lnc-AGPS-3	chr2:178567216-178567477	ENSG00000229941.1

No data

Variant related genes	Relation type
ENSG00000229941	TF binding region
PDE11A	TF binding region
ENSG00000229941	CpG island
PDE11A	CpG island
ENSG00000128655	chromatin interactions
ENSG00000018510	chromatin interactions
ENSG00000213963	chromatin interactions
ENSG00000116044	chromatin interactions
ENSG00000196659	chromatin interactions
ENSG00000229941	chromatin interactions

Extended variants
information (count: 954 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6433691	chr2:178551958-178551959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573879703	chr2:178551971-178551972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78237516	chr2:178551982-178551983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559615395	chr2:178552028-178552029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113610012	chr2:178552059-178552060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11310982	chr2:178552072-178552073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528798984	chr2:178552117-178552118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552059186	chr2:178552132-178552133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145177343	chr2:178552137-178552138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77893596	chr2:178552164-178552165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139024865	chr2:178552173-178552174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569798551	chr2:178552216-178552217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76563834	chr2:178552233-178552234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74385454	chr2:178552234-178552235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149420034	chr2:178552252-178552253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193271790	chr2:178552255-178552256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565894030	chr2:178552289-178552290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534568424	chr2:178552305-178552306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558055461	chr2:178552383-178552384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141110343	chr2:178552416-178552417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183287877	chr2:178552421-178552422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537487976	chr2:178552428-178552429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557013485	chr2:178552438-178552439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573842753	chr2:178552453-178552454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542802958	chr2:178552538-178552539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559478249	chr2:178552543-178552544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553567686	chr2:178552564-178552565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188662307	chr2:178552654-178552655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542206427	chr2:178552699-178552700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34054341	chr2:178552760-178552761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144788507	chr2:178552774-178552775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13032794	chr2:178552788-178552789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532773503	chr2:178552815-178552816	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549797735	chr2:178552836-178552837	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192692996	chr2:178552863-178552864	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528957772	chr2:178552883-178552884	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111715714	chr2:178552885-178552886	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565852132	chr2:178552941-178552942	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115210447	chr2:178552965-178552966	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551370224	chr2:178553012-178553013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559115870	chr2:178553030-178553031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372742767	chr2:178553031-178553032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544861813	chr2:178553041-178553042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77068733	chr2:178553113-178553114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556974871	chr2:178553120-178553121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs78536650	chr2:178553183-178553184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs10175970	chr2:178553238-178553239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553070289	chr2:178553261-178553262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148559414	chr2:178553265-178553266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562117028	chr2:178553267-178553268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178536600-178556000	Weak transcription	Pancreas	Pancrea
2	chr2:178544600-178552600	Weak transcription	Fetal Intestine Small	intestine
3	chr2:178546800-178554400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:178547000-178552800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:178547400-178554400	Weak transcription	Fetal Kidney	kidney
6	chr2:178549400-178554400	Weak transcription	K562	blood
7	chr2:178550000-178554200	Weak transcription	Stomach Mucosa	stomach
8	chr2:178550000-178557000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr2:178550400-178555800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:178552600-178552800	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr2:178552600-178553000	Enhancers	Fetal Intestine Small	intestine
12	chr2:178552800-178553000	Enhancers	Fetal Intestine Large	intestine
13	chr2:178552800-178553000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
14	chr2:178552800-178553200	Enhancers	Duodenum Mucosa	Duodenum
15	chr2:178552800-178553200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr2:178552800-178554000	Enhancers	Dnd41	blood
17	chr2:178553000-178553400	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr2:178553000-178554200	Weak transcription	Fetal Intestine Small	intestine
19	chr2:178553000-178557000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:178553000-178557000	Weak transcription	Fetal Intestine Large	intestine
21	chr2:178553200-178557000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr2:178553200-178557200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr2:178553400-178554400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr2:178553800-178555200	Enhancers	Fetal Thymus	thymus
25	chr2:178554000-178554800	Flanking Active TSS	Dnd41	blood
26	chr2:178554000-178555200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr2:178554200-178555000	Enhancers	Fetal Intestine Small	intestine
28	chr2:178554200-178555000	Enhancers	Stomach Mucosa	stomach
29	chr2:178554200-178555400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:178554400-178554600	Enhancers	Liver	Liver
31	chr2:178554400-178554600	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:178554400-178554800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:178554400-178554800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr2:178554400-178554800	Enhancers	Thymus	Thymus
35	chr2:178554400-178555000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr2:178554400-178555000	Enhancers	Fetal Kidney	kidney
37	chr2:178554400-178555000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr2:178554400-178555200	Enhancers	K562	blood
39	chr2:178554400-178555600	Enhancers	Primary hematopoietic stem cells	blood
40	chr2:178554600-178554800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:178554600-178554800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:178554600-178554800	Enhancers	Gastric	stomach
43	chr2:178554600-178555400	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr2:178554600-178556400	Weak transcription	Liver	Liver
45	chr2:178554800-178555200	Enhancers	Dnd41	blood
46	chr2:178554800-178556000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:178554800-178556400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:178554800-178557400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:178554800-178557800	Weak transcription	Gastric	stomach
50	chr2:178555000-178555400	Weak transcription	Fetal Kidney	kidney

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