Variant report

Variant	esv1795156
Chromosome Location	chr2:112033530-112188506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1232)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:43)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
3	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
4	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
5	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
6	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
7	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
8	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
9	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
12	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
13	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
14	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
15	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
16	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
17	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
18	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
19	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
20	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
21	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
22	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
23	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
24	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
25	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
26	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
27	BATF	chr2:112049833-112050062	GM12878	blood:	n/a	n/a
28	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
29	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
30	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
31	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
32	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
33	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
34	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
35	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
36	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
37	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
38	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:112183223-112183810	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:112182226-112182918	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:112186983-112187434	GM12878	blood:	n/a	chr2:112187266-112187275
44	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
45	BCL11A	chr2:112182331-112182639	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
48	BCL3	chr2:112183366-112183629	GM12878	blood:	n/a	n/a
49	BHLHE40	chr2:112165402-112165622	K562	blood:	n/a	n/a
50	BHLHE40	chr2:112168058-112168310	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124380-112124430	GM12891	blood:	n/a
2	chr2:112124118-112124168	BE2_C	brain:	n/a
3	chr2:112124380-112124430	A549	lung:	n/a
4	chr2:112124380-112124430	PANC-1	pancreas:	n/a
5	chr2:112124118-112124168	HCPEpiC	choroid plexus:	n/a
6	chr2:112124380-112124430	SKMC	muscle:	n/a
7	chr2:112124118-112124168	BJ	skin:	n/a
8	chr2:112124118-112124168	NHBE	bronchial:	n/a
9	chr2:112124380-112124430	HRCEpiC	kidney:	n/a
10	chr2:112124118-112124168	Hepatocyte	liver:	n/a
11	chr2:112124118-112124168	AG09309	skin:	n/a
12	chr2:112124380-112124430	HL-60	blood:	n/a
13	chr2:112124380-112124430	NH-A	brain:	n/a
14	chr2:112124118-112124168	HCF	heart:	n/a
15	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
16	chr2:112124380-112124430	HepG2	liver:	n/a
17	chr2:112124118-112124168	PANC-1	pancreas:	n/a
18	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
19	chr2:112124380-112124430	Hepatocyte	liver:	n/a
20	chr2:112124118-112124168	HCM	heart:	n/a
21	chr2:112124118-112124168	A549	lung:	n/a
22	chr2:112124118-112124168	T-47D	breast:	n/a
23	chr2:112124118-112124168	Jurkat	blood:	n/a
24	chr2:112124118-112124168	IMR90	lung:	fetal
25	chr2:112124118-112124168	SAEC	small airway:	n/a
26	chr2:112124118-112124168	GM12878	blood:	n/a
27	chr2:112124118-112124168	AG04449	skin:	fetal
28	chr2:112124380-112124430	U87	brain:	n/a
29	chr2:112124118-112124168	CMK	blood:	n/a
30	chr2:112124380-112124430	HRE	kidney:	n/a
31	chr2:112124380-112124430	NB4	blood:	n/a
32	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
33	chr2:112124380-112124430	RPTEC	kidney:	n/a
34	chr2:112124380-112124430	HRPEpiC	eye:	n/a
35	chr2:112124380-112124430	CMK	blood:	n/a
36	chr2:112124380-112124430	HIPEpiC	eye:	n/a
37	chr2:112124118-112124168	AG10803	skin:	n/a
38	chr2:112124118-112124168	HRCEpiC	kidney:	n/a
39	chr2:112124118-112124168	MCF-7	breast:	n/a
40	chr2:112124380-112124430	HMEC	breast:	n/a
41	chr2:112124380-112124430	SK-N-MC	brain:	n/a
42	chr2:112124118-112124168	ECC-1	luminal epithelium:	n/a
43	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
44	chr2:112124380-112124430	GM12878	blood:	n/a
45	chr2:112124380-112124430	NT2-D1	testis:	n/a
46	chr2:112124118-112124168	PFSK-1	brain:	n/a
47	chr2:112124380-112124430	HCF	heart:	n/a
48	chr2:112124118-112124168	HepG2	liver:	n/a
49	chr2:112124380-112124430	Jurkat	blood:	n/a
50	chr2:112124118-112124168	PrEC	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
2	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
3	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
2	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
3	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
5	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
6	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
7	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
8	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
9	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
10	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
11	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
12	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
14	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
15	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
16	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
17	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
18	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
19	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
20	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
22	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
23	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
24	lnc-BCL2L11-2	chr2:112037444-112037486	XLOC_001624
25	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
26	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
27	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624
28	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
29	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
31	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
32	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
33	lnc-AC108463.1-3	chr2:112033908-112033997	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
35	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
36	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
37	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
38	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
39	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
40	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
41	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
42	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
43	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
KLHL24	miRNA target sites
ASCC3	miRNA target sites
ITSN2	miRNA target sites

Extended variants
information (count: 3871 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3871 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562665799	chr2:112033532-112033533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146595744	chr2:112033538-112033539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531413759	chr2:112033549-112033550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141055367	chr2:112033569-112033570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551604276	chr2:112033586-112033587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571443964	chr2:112033602-112033603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527621271	chr2:112033609-112033610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547396629	chr2:112033634-112033635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567296068	chr2:112033651-112033652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201054945	chr2:112033743-112033744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536319343	chr2:112033780-112033781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555994773	chr2:112033808-112033809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376144599	chr2:112033821-112033822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538856911	chr2:112033833-112033834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1710469	chr2:112033877-112033878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559145301	chr2:112033957-112033958	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs572632915	chr2:112033988-112033989	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs541351242	chr2:112033996-112033997	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs554511315	chr2:112033997-112033998	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs574507223	chr2:112034005-112034006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181021814	chr2:112034043-112034044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369585081	chr2:112034051-112034052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543470774	chr2:112034057-112034058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199817991	chr2:112034232-112034233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563633327	chr2:112034402-112034403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532684409	chr2:112034407-112034408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386649181	chr2:112034429-112034430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147048614	chr2:112034430-112034431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4849528	chr2:112034433-112034434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1710470	chr2:112034434-112034435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113826161	chr2:112034444-112034445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147014411	chr2:112034447-112034448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374540282	chr2:112034489-112034490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1706157	chr2:112034507-112034508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186055538	chr2:112034517-112034518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1877329	chr2:112034550-112034551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569640163	chr2:112034553-112034554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs925956	chr2:112034633-112034634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs558860620	chr2:112034669-112034670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565952749	chr2:112034670-112034671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534951607	chr2:112034687-112034688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554852238	chr2:112034719-112034720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370422441	chr2:112034720-112034721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537046171	chr2:112034730-112034731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557361799	chr2:112034736-112034737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577245616	chr2:112034739-112034740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80083464	chr2:112034746-112034747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546301707	chr2:112034756-112034757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564896350	chr2:112034775-112034776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540451213	chr2:112034809-112034810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:997 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112008600-112048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:112020600-112048000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:112023400-112046400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:112025000-112034400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:112025800-112037800	Weak transcription	HSMM	muscle
7	chr2:112031400-112036000	Weak transcription	Pancreas	Pancrea
8	chr2:112033400-112034200	Enhancers	Left Ventricle	heart
9	chr2:112034200-112034800	Weak transcription	Left Ventricle	heart
10	chr2:112034800-112035000	Enhancers	Left Ventricle	heart
11	chr2:112036000-112036200	Enhancers	Pancreas	Pancrea
12	chr2:112044400-112046600	Weak transcription	Pancreas	Pancrea
13	chr2:112045400-112045600	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr2:112045400-112045800	Enhancers	NHEK	skin
15	chr2:112045400-112046000	Enhancers	HMEC	breast
16	chr2:112045600-112046200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:112045800-112047600	Weak transcription	NHEK	skin
18	chr2:112046000-112046400	Weak transcription	HMEC	breast
19	chr2:112046200-112046400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr2:112046400-112046600	Enhancers	HMEC	breast
21	chr2:112046400-112046800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:112046400-112047000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:112046400-112047800	Enhancers	Placenta	Placenta
24	chr2:112046400-112048600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr2:112046400-112057400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:112046600-112047800	Weak transcription	HMEC	breast
27	chr2:112047000-112047400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr2:112047000-112048400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:112047600-112047800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:112047600-112048800	Enhancers	NHEK	skin
31	chr2:112047800-112048600	Weak transcription	Placenta	Placenta
32	chr2:112047800-112049600	Enhancers	HMEC	breast
33	chr2:112047800-112052400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:112048000-112048800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:112048400-112048600	Enhancers	Pancreas	Pancrea
36	chr2:112048400-112048800	Enhancers	Liver	Liver
37	chr2:112048400-112049000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:112048600-112048800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr2:112048600-112048800	Enhancers	Placenta	Placenta
40	chr2:112048600-112049400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr2:112048600-112049600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:112048600-112051000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:112048800-112049200	Weak transcription	Liver	Liver
44	chr2:112048800-112049400	Weak transcription	Placenta	Placenta
45	chr2:112048800-112049600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr2:112048800-112049800	Enhancers	HSMMtube	muscle
47	chr2:112048800-112069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:112049000-112050600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:112049200-112049800	Enhancers	Liver	Liver
50	chr2:112049400-112049600	Enhancers	Brain Inferior Temporal Lobe	brain

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