Variant report

Variant	esv1794638
Chromosome Location	chr2:112012312-112156243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:928)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:40)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr2:112078700-112078866	K562	blood:	n/a	n/a
4	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
5	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
6	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
7	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
8	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
9	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
10	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
11	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
12	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
13	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
14	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
15	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
16	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
17	BATF	chr2:112029454-112029812	GM12878	blood:	n/a	chr2:112029663-112029674
18	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
19	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
20	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
21	BATF	chr2:112029496-112029836	GM12878	blood:	n/a	chr2:112029663-112029674
22	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
23	BATF	chr2:112049833-112050062	GM12878	blood:	n/a	n/a
24	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
25	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
26	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
27	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
31	BHLHE40	chr2:112050013-112050384	HepG2	liver:	n/a	n/a
32	BHLHE40	chr2:112078723-112078845	K562	blood:	n/a	n/a
33	BHLHE40	chr2:112133109-112133309	K562	blood:	n/a	n/a
34	CBX3	chr2:112116534-112117202	K562	blood:	n/a	n/a
35	CBX3	chr2:112078409-112078978	K562	blood:	n/a	n/a
36	CBX3	chr2:112077663-112078252	K562	blood:	n/a	n/a
37	CBX3	chr2:112104099-112104804	K562	blood:	n/a	n/a
38	CBX3	chr2:112040510-112040835	K562	blood:	n/a	n/a
39	CBX3	chr2:112123477-112124140	K562	blood:	n/a	n/a
40	CBX3	chr2:112117660-112118021	K562	blood:	n/a	n/a
41	CBX3	chr2:112109931-112110500	K562	blood:	n/a	n/a
42	CBX3	chr2:112116542-112117069	K562	blood:	n/a	n/a
43	CBX3	chr2:112109995-112110254	K562	blood:	n/a	n/a
44	CBX3	chr2:112139460-112139855	K562	blood:	n/a	n/a
45	CBX3	chr2:112105200-112105741	K562	blood:	n/a	n/a
46	CBX3	chr2:112097460-112097828	K562	blood:	n/a	n/a
47	CBX3	chr2:112097533-112097824	K562	blood:	n/a	n/a
48	CEBPB	chr2:112078650-112078865	A549	lung:	n/a	n/a
49	CEBPB	chr2:112072831-112073009	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:112132956-112133341	K562	blood:	n/a	chr2:112133186-112133195 chr2:112133185-112133196 chr2:112133184-112133197 chr2:112133186-112133195 chr2:112133184-112133197 chr2:112133186-112133195

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	HMEC	breast:	n/a
2	chr2:112124118-112124168	GM19239	blood:	n/a
3	chr2:112124118-112124168	GM12891	blood:	n/a
4	chr2:112124380-112124430	A549	lung:	n/a
5	chr2:112124380-112124430	RPTEC	kidney:	n/a
6	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
7	chr2:112124380-112124430	MCF-7	breast:	n/a
8	chr2:112124118-112124168	HIPEpiC	eye:	n/a
9	chr2:112124118-112124168	HEK293	kidney:	embryo
10	chr2:112124380-112124430	PANC-1	pancreas:	n/a
11	chr2:112124118-112124168	AG04449	skin:	fetal
12	chr2:112124380-112124430	Jurkat	blood:	n/a
13	chr2:112124380-112124430	ECC-1	luminal epithelium:	n/a
14	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
15	chr2:112124118-112124168	HCPEpiC	choroid plexus:	n/a
16	chr2:112124380-112124430	SAEC	small airway:	n/a
17	chr2:112124118-112124168	SK-N-MC	brain:	n/a
18	chr2:112124380-112124430	IMR90	lung:	fetal
19	chr2:112124118-112124168	HCM	heart:	n/a
20	chr2:112124118-112124168	AG04450	lung:	fetal
21	chr2:112124118-112124168	NHDF-neo	bronchial:	n/a
22	chr2:112124380-112124430	T-47D	breast:	n/a
23	chr2:112124118-112124168	PFSK-1	brain:	n/a
24	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
25	chr2:112124118-112124168	A549	lung:	n/a
26	chr2:112124118-112124168	SK-N-SH_RA	brain:	n/a
27	chr2:112124380-112124430	NH-A	brain:	n/a
28	chr2:112124380-112124430	HAEpiC	amniotic membrane:	n/a
29	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
30	chr2:112124380-112124430	SK-N-SH_RA	brain:	n/a
31	chr2:112124380-112124430	HRE	kidney:	n/a
32	chr2:112124380-112124430	HRPEpiC	eye:	n/a
33	chr2:112124380-112124430	BE2_C	brain:	n/a
34	chr2:112124118-112124168	AG09319	gingival:	n/a
35	chr2:112124380-112124430	GM12891	blood:	n/a
36	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo
37	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:112124380-112124430	ProgFib	skin:	n/a
39	chr2:112124118-112124168	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:112124380-112124430	HMEC	breast:	n/a
41	chr2:112124380-112124430	AG04450	lung:	fetal
42	chr2:112124380-112124430	SK-N-MC	brain:	n/a
43	chr2:112124380-112124430	AG04449	skin:	fetal
44	chr2:112124118-112124168	HAEpiC	amniotic membrane:	n/a
45	chr2:112124118-112124168	MCF-7	breast:	n/a
46	chr2:112124380-112124430	HepG2	liver:	n/a
47	chr2:112124380-112124430	GM12878	blood:	n/a
48	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
49	chr2:112124380-112124430	SK-N-SH	brain:	n/a
50	chr2:112124380-112124430	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
2	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
3	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
4	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
5	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
6	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
7	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
8	lnc-AC108463.1-4	chr2:112024445-112025050	ENSG00000270190.1
9	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
10	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
11	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
12	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
13	lnc-BCL2L11-2	chr2:112022860-112023040	XLOC_001624
14	lnc-AC108463.1-4	chr2:112024419-112025062	NONHSAT073632
15	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624
16	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
17	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
18	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
19	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
20	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
22	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
23	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
24	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
25	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
26	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
28	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
29	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
30	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
31	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
32	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
33	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
34	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
35	lnc-BCL2L11-2	chr2:112037444-112037486	XLOC_001624
36	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
37	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
38	lnc-AC108463.1-3	chr2:112033908-112033997	ENSG00000172965.6
39	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
40	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6

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

No data

Variant related genes	Relation type
ENSG00000270190	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000229118	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000270190	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000229118	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
KLHL24	miRNA target sites
ITSN2	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 3587 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3587 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55767262	chr2:112012312-112012313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536468500	chr2:112012325-112012326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77348742	chr2:112012338-112012339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575280025	chr2:112012396-112012397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541125933	chr2:112012420-112012421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148874165	chr2:112012429-112012430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577223644	chr2:112012486-112012487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371554698	chr2:112012506-112012507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560206653	chr2:112012593-112012594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186475034	chr2:112012614-112012615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376101187	chr2:112012635-112012636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57874285	chr2:112012672-112012673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs57707030	chr2:112012682-112012683	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551906967	chr2:112012727-112012728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1706200	chr2:112012742-112012743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115415330	chr2:112012756-112012757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529609945	chr2:112012757-112012758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1706199	chr2:112012771-112012772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527701163	chr2:112012780-112012781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547742665	chr2:112012830-112012831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138514695	chr2:112012834-112012835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566238277	chr2:112012843-112012844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530404884	chr2:112012865-112012866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200354019	chr2:112012898-112012899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569914204	chr2:112012907-112012908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369632144	chr2:112012989-112012990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62160426	chr2:112013016-112013017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538803812	chr2:112013062-112013063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533906814	chr2:112013140-112013141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553559711	chr2:112013158-112013159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557443196	chr2:112013164-112013165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570978168	chr2:112013325-112013326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533567699	chr2:112013347-112013348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62160427	chr2:112013373-112013374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201848529	chr2:112013535-112013536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55778104	chr2:112013606-112013607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149614465	chr2:112013625-112013626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1710483	chr2:112013632-112013633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201338570	chr2:112013747-112013748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576311611	chr2:112013763-112013764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545189732	chr2:112013765-112013766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565399986	chr2:112013838-112013839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527764053	chr2:112014437-112014438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556722926	chr2:112014526-112014527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111243750	chr2:112014693-112014694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541101516	chr2:112014736-112014737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139852707	chr2:112014835-112014836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530374906	chr2:112014869-112014870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550453980	chr2:112014989-112014990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569976530	chr2:112015305-112015306	Weak transcription	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:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112005600-112015800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:112006200-112020200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:112008600-112048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:112009200-112022600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:112010200-112015400	Weak transcription	HMEC	breast
6	chr2:112010600-112024600	Weak transcription	HSMMtube	muscle
7	chr2:112015400-112016600	Enhancers	HMEC	breast
8	chr2:112015800-112016000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:112016000-112016400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:112016000-112016400	Enhancers	NHEK	skin
11	chr2:112016200-112016600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:112016400-112016600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:112016600-112029000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:112019000-112019200	Enhancers	Ovary	ovary
15	chr2:112019200-112024200	Weak transcription	Ovary	ovary
16	chr2:112019200-112032600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:112020200-112020600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:112020200-112020600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:112020200-112020600	Enhancers	Fetal Stomach	stomach
20	chr2:112020200-112020600	Enhancers	NHLF	lung
21	chr2:112020400-112020600	Enhancers	Fetal Muscle Trunk	muscle
22	chr2:112020400-112020600	Enhancers	Lung	lung
23	chr2:112020600-112021800	Weak transcription	NHLF	lung
24	chr2:112020600-112024200	Weak transcription	Lung	lung
25	chr2:112020600-112024600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:112020600-112048000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr2:112022000-112022200	Enhancers	NHLF	lung
28	chr2:112022400-112022600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:112022600-112022800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:112022600-112023000	Enhancers	Fetal Muscle Trunk	muscle
31	chr2:112022600-112023400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:112022800-112031200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:112023400-112046400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:112024000-112024400	Enhancers	Right Ventricle	heart
35	chr2:112024200-112025000	Enhancers	Lung	lung
36	chr2:112024200-112025200	Enhancers	Fetal Lung	lung
37	chr2:112024200-112025200	Enhancers	Ovary	ovary
38	chr2:112024200-112025200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr2:112024200-112025200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:112024200-112025400	Enhancers	Pancreas	Pancrea
41	chr2:112024200-112025600	Enhancers	Liver	Liver
42	chr2:112024200-112025600	Enhancers	Fetal Heart	heart
43	chr2:112024400-112025400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:112024600-112024800	Enhancers	HSMMtube	muscle
45	chr2:112024600-112025000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:112024600-112025000	Enhancers	Gastric	stomach
47	chr2:112024600-112025000	Enhancers	Stomach Mucosa	stomach
48	chr2:112024800-112025000	Enhancers	Fetal Muscle Trunk	muscle
49	chr2:112024800-112026000	Weak transcription	HSMMtube	muscle
50	chr2:112025000-112034400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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