Variant report

Variant	nsv1005991
Chromosome Location	chr2:178550049-178577002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 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	chr2:178557491-178557668	K562	blood:	n/a	n/a
2	ARID3A	chr2:178558288-178559366	K562	blood:	n/a	n/a
3	ARID3A	chr2:178554400-178554623	K562	blood:	n/a	n/a
4	ARID3A	chr2:178556633-178557685	HepG2	liver:	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	chr2:178558039-178559104	K562	blood:	n/a	n/a
9	BHLHE40	chr2:178557739-178557741	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	chr2:178557271-178557521	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:178557263-178557501	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:178550913-178551154	K562	blood:	n/a	chr2:178551070-178551081
16	CEBPB	chr2:178569543-178569609	HepG2	liver:	n/a	chr2:178569565-178569576
17	CEBPB	chr2:178550933-178551144	A549	lung:	n/a	chr2:178551070-178551081
18	CEBPB	chr2:178558569-178558614	H1-hESC	embryonic stem cell:	n/a	chr2:178558576-178558587
19	CEBPB	chr2:178550933-178551169	HepG2	liver:	n/a	chr2:178551070-178551081
20	CEBPB	chr2:178557191-178557717	A549	lung:	n/a	chr2:178557583-178557595
21	CEBPB	chr2:178558415-178558716	HepG2	liver:	n/a	chr2:178558576-178558587
22	CEBPB	chr2:178557275-178557602	A549	lung:	n/a	chr2:178557583-178557595
23	CEBPB	chr2:178550983-178551107	H1-hESC	embryonic stem cell:	n/a	chr2:178551070-178551081
24	CEBPB	chr2:178558416-178558685	IMR90	lung:	n/a	chr2:178558576-178558587
25	CEBPB	chr2:178558429-178558729	A549	lung:	n/a	chr2:178558576-178558587
26	CEBPB	chr2:178558315-178559143	K562	blood:	n/a	chr2:178558576-178558587
27	CEBPB	chr2:178558425-178559027	K562	blood:	n/a	chr2:178558576-178558587
28	CEBPB	chr2:178551012-178551128	IMR90	lung:	n/a	chr2:178551070-178551081
29	CEBPB	chr2:178558399-178559087	K562	blood:	n/a	chr2:178558576-178558587
30	CEBPB	chr2:178557240-178557599	HepG2	liver:	n/a	chr2:178557583-178557595
31	CEBPD	chr2:178558470-178559144	K562	blood:	n/a	n/a
32	CEBPD	chr2:178558362-178559103	K562	blood:	n/a	n/a
33	CTCF	chr2:178557640-178557790	AG09309	skin:	n/a	n/a
34	CTCF	chr2:178556080-178556230	RPTEC	kidney:	n/a	n/a
35	CTCF	chr2:178557600-178557750	HEK293	kidney:	n/a	n/a
36	CTCF	chr2:178555980-178556130	GM12865	blood:	n/a	chr2:178555992-178556001
37	CTCF	chr2:178556040-178556190	GM12865	blood:	n/a	n/a
38	CTCF	chr2:178557600-178557750	AG10803	skin:	n/a	n/a
39	CTCF	chr2:178557700-178557850	RPTEC	kidney:	n/a	n/a
40	CTCF	chr2:178557620-178557770	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr2:178557640-178557790	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr2:178555944-178556211	K562	blood:	n/a	chr2:178555992-178556001
43	CTCF	chr2:178557686-178557763	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:178557667-178557794	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr2:178557600-178557750	HCM	heart:	n/a	n/a
46	CTCF	chr2:178557700-178557850	GM06990	blood:	n/a	n/a
47	CTCF	chr2:178557686-178557743	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:178557680-178557830	NHEK	skin:	n/a	n/a
49	CTCF	chr2:178556040-178556190	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:178555980-178556130	GM12866	blood:	n/a	chr2:178555992-178556001

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178556488-178556538	PANC-1	pancreas:	n/a
2	chr2:178556488-178556538	PFSK-1	brain:	n/a
3	chr2:178556488-178556538	AG09309	skin:	n/a
4	chr2:178556488-178556538	ECC-1	luminal epithelium:	n/a
5	chr2:178556488-178556538	AG09319	gingival:	n/a
6	chr2:178556488-178556538	HRPEpiC	eye:	n/a
7	chr2:178556488-178556538	HCT-116	colon:	n/a
8	chr2:178556488-178556538	HNPCEpiC	eye:	n/a
9	chr2:178556488-178556538	Jurkat	blood:	n/a
10	chr2:178556488-178556538	HRE	kidney:	n/a
11	chr2:178556488-178556538	ProgFib	skin:	n/a
12	chr2:178556488-178556538	NB4	blood:	n/a
13	chr2:178556488-178556538	AoSMC	blood vessel:	n/a
14	chr2:178556488-178556538	MCF10A-Er-Src	breast:	n/a
15	chr2:178556488-178556538	GM12891	blood:	n/a
16	chr2:178556488-178556538	HepG2	liver:	n/a
17	chr2:178556488-178556538	HIPEpiC	eye:	n/a
18	chr2:178556488-178556538	HMEC	breast:	n/a
19	chr2:178556488-178556538	HL-60	blood:	n/a
20	chr2:178556488-178556538	GM19239	blood:	n/a
21	chr2:178556488-178556538	BJ	skin:	n/a
22	chr2:178556488-178556538	HCPEpiC	choroid plexus:	n/a
23	chr2:178556488-178556538	SKMC	muscle:	n/a
24	chr2:178556488-178556538	Caco-2	colon:	n/a
25	chr2:178556488-178556538	SAEC	small airway:	n/a
26	chr2:178556488-178556538	NHBE	bronchial:	n/a
27	chr2:178556488-178556538	GM06990	blood:	n/a
28	chr2:178556488-178556538	CMK	blood:	n/a
29	chr2:178556488-178556538	HAEpiC	amniotic membrane:	n/a
30	chr2:178556488-178556538	Hela-S3	cervix:	n/a
31	chr2:178556488-178556538	U87	brain:	n/a
32	chr2:178556488-178556538	SK-N-SH_RA	brain:	n/a
33	chr2:178556488-178556538	A549	lung:	n/a
34	chr2:178556488-178556538	RPTEC	kidney:	n/a
35	chr2:178556488-178556538	NHDF-neo	bronchial:	n/a
36	chr2:178556488-178556538	MCF-7	breast:	n/a
37	chr2:178556488-178556538	LNCaP	prostate:	n/a
38	chr2:178556488-178556538	NT2-D1	testis:	n/a
39	chr2:178556488-178556538	K562	blood:	n/a
40	chr2:178556488-178556538	HCM	heart:	n/a
41	chr2:178556488-178556538	HCF	heart:	n/a
42	chr2:178556488-178556538	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:178556488-178556538	BE2_C	brain:	n/a
44	chr2:178556488-178556538	AG04450	lung:	fetal
45	chr2:178556488-178556538	T-47D	breast:	n/a
46	chr2:178556488-178556538	PrEC	prostate:	n/a
47	chr2:178556488-178556538	ovcar-3	ovarian:	n/a
48	chr2:178556488-178556538	IMR90	lung:	fetal
49	chr2:178556488-178556538	SK-N-SH	brain:	n/a
50	chr2:178556488-178556538	GM12892	blood:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPS-3	chr2:178563157-178563299	ENSG00000229941.1
2	lnc-AGPS-3	chr2:178563218-178563299	ENSG00000229941.1
3	lnc-AGPS-3	chr2:178565822-178565956	ENSG00000229941.1
4	lnc-AGPS-3	chr2:178567216-178567477	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
ENSG00000229941	chromatin interactions
ENSG00000196659	chromatin interactions
ENSG00000213963	chromatin interactions
ENSG00000128655	chromatin interactions
ENSG00000116044	chromatin interactions
ENSG00000018510	chromatin interactions

Extended variants
information (count: 1043 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149997437	chr2:178550049-178550050	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs556604471	chr2:178550055-178550056	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs575134392	chr2:178550151-178550152	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537481621	chr2:178550161-178550162	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs111884108	chr2:178550169-178550170	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546975212	chr2:178550180-178550181	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532868194	chr2:178550182-178550183	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574218568	chr2:178550194-178550195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192962518	chr2:178550211-178550212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540021357	chr2:178550227-178550228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185384085	chr2:178550228-178550229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576985814	chr2:178550240-178550241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546032417	chr2:178550255-178550256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562650283	chr2:178550269-178550270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148392753	chr2:178550278-178550279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397955190	chr2:178550286-178550287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189444579	chr2:178550292-178550293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536161198	chr2:178550300-178550301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78779101	chr2:178550307-178550308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562144258	chr2:178550320-178550321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192926429	chr2:178550326-178550327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547917902	chr2:178550335-178550336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77885212	chr2:178550338-178550339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539663616	chr2:178550340-178550341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550437150	chr2:178550343-178550344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570285036	chr2:178550369-178550370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183453881	chr2:178550399-178550400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554186061	chr2:178550400-178550401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574104576	chr2:178550419-178550420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188330290	chr2:178550430-178550431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553472758	chr2:178550436-178550437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112975202	chr2:178550477-178550478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545712847	chr2:178550501-178550502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562779047	chr2:178550509-178550510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10183838	chr2:178550541-178550542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs144556216	chr2:178550546-178550547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562019375	chr2:178550547-178550548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181841474	chr2:178550550-178550551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527686759	chr2:178550580-178550581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541506234	chr2:178550581-178550582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114881106	chr2:178550584-178550585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74625156	chr2:178550594-178550595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61260452	chr2:178550624-178550625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570321447	chr2:178550646-178550647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529505212	chr2:178550660-178550661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549269372	chr2:178550696-178550697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533401077	chr2:178550755-178550756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533558181	chr2:178550793-178550794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553815065	chr2:178550831-178550832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551679840	chr2:178550906-178550907	Weak transcription	n/a	n/a	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:179 , 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	chr2:178549400-178550200	Enhancers	HepG2	liver
7	chr2:178549400-178554400	Weak transcription	K562	blood
8	chr2:178549600-178550400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:178550000-178554200	Weak transcription	Stomach Mucosa	stomach
10	chr2:178550000-178557000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr2:178550400-178555800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:178552600-178552800	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr2:178552600-178553000	Enhancers	Fetal Intestine Small	intestine
14	chr2:178552800-178553000	Enhancers	Fetal Intestine Large	intestine
15	chr2:178552800-178553000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
16	chr2:178552800-178553200	Enhancers	Duodenum Mucosa	Duodenum
17	chr2:178552800-178553200	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr2:178552800-178554000	Enhancers	Dnd41	blood
19	chr2:178553000-178553400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr2:178553000-178554200	Weak transcription	Fetal Intestine Small	intestine
21	chr2:178553000-178557000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:178553000-178557000	Weak transcription	Fetal Intestine Large	intestine
23	chr2:178553200-178557000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:178553200-178557200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr2:178553400-178554400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:178553800-178555200	Enhancers	Fetal Thymus	thymus
27	chr2:178554000-178554800	Flanking Active TSS	Dnd41	blood
28	chr2:178554000-178555200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:178554200-178555000	Enhancers	Fetal Intestine Small	intestine
30	chr2:178554200-178555000	Enhancers	Stomach Mucosa	stomach
31	chr2:178554200-178555400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:178554400-178554600	Enhancers	Liver	Liver
33	chr2:178554400-178554600	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr2:178554400-178554800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:178554400-178554800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr2:178554400-178554800	Enhancers	Thymus	Thymus
37	chr2:178554400-178555000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:178554400-178555000	Enhancers	Fetal Kidney	kidney
39	chr2:178554400-178555000	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr2:178554400-178555200	Enhancers	K562	blood
41	chr2:178554400-178555600	Enhancers	Primary hematopoietic stem cells	blood
42	chr2:178554600-178554800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:178554600-178554800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:178554600-178554800	Enhancers	Gastric	stomach
45	chr2:178554600-178555400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr2:178554600-178556400	Weak transcription	Liver	Liver
47	chr2:178554800-178555200	Enhancers	Dnd41	blood
48	chr2:178554800-178556000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:178554800-178556400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:178554800-178557400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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