Variant report

Variant	esv2757826
Chromosome Location	chr2:114074949-114253780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2122)
CpG islands
(count:795)
Chromatin interactive
region (count:39)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2122 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114181075-114181226	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:114165283-114165660	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114165284-114165610	K562	blood:	n/a	n/a
4	ARID3A	chr2:114147862-114148323	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:114127759-114128394	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:114147934-114148353	K562	blood:	n/a	n/a
7	ATF1	chr2:114101429-114101681	K562	blood:	n/a	n/a
8	ATF1	chr2:114075345-114075373	K562	blood:	n/a	n/a
9	ATF1	chr2:114195252-114195468	K562	blood:	n/a	n/a
10	ATF2	chr2:114147524-114148275	GM12878	blood:	n/a	n/a
11	ATF2	chr2:114134096-114134875	GM12878	blood:	n/a	n/a
12	ATF2	chr2:114134165-114134981	GM12878	blood:	n/a	n/a
13	ATF3	chr2:114128032-114128470	A549	lung:	n/a	n/a
14	ATF3	chr2:114147873-114148254	GM12878	blood:	n/a	n/a
15	ATF3	chr2:114086463-114087004	A549	lung:	n/a	n/a
16	ATF3	chr2:114086473-114087012	A549	lung:	n/a	n/a
17	ATF3	chr2:114195215-114195323	K562	blood:	n/a	n/a
18	BATF	chr2:114214368-114214841	GM12878	blood:	n/a	n/a
19	BATF	chr2:114194968-114195790	GM12878	blood:	n/a	chr2:114195333-114195346
20	BATF	chr2:114188894-114189247	GM12878	blood:	n/a	n/a
21	BATF	chr2:114188935-114190118	GM12878	blood:	n/a	chr2:114189910-114189918
22	BATF	chr2:114242853-114243066	GM12878	blood:	n/a	n/a
23	BATF	chr2:114196999-114197200	GM12878	blood:	n/a	n/a
24	BATF	chr2:114122973-114123368	GM12878	blood:	n/a	n/a
25	BATF	chr2:114134468-114134876	GM12878	blood:	n/a	n/a
26	BATF	chr2:114179478-114179679	GM12878	blood:	n/a	n/a
27	BATF	chr2:114206835-114207033	GM12878	blood:	n/a	n/a
28	BATF	chr2:114221639-114221843	GM12878	blood:	n/a	n/a
29	BATF	chr2:114206782-114207175	GM12878	blood:	n/a	n/a
30	BATF	chr2:114173977-114174745	GM12878	blood:	n/a	n/a
31	BATF	chr2:114194949-114195748	GM12878	blood:	n/a	chr2:114195333-114195346
32	BATF	chr2:114189261-114190171	GM12878	blood:	n/a	chr2:114189910-114189918
33	BATF	chr2:114253690-114253875	GM12878	blood:	n/a	n/a
34	BATF	chr2:114190291-114190748	GM12878	blood:	n/a	n/a
35	BATF	chr2:114196004-114196344	GM12878	blood:	n/a	n/a
36	BATF	chr2:114175312-114175602	GM12878	blood:	n/a	chr2:114175554-114175563
37	BATF	chr2:114188216-114188558	GM12878	blood:	n/a	n/a
38	BATF	chr2:114134508-114134842	GM12878	blood:	n/a	n/a
39	BATF	chr2:114147578-114148177	GM12878	blood:	n/a	n/a
40	BATF	chr2:114190256-114190764	GM12878	blood:	n/a	n/a
41	BATF	chr2:114123077-114123326	GM12878	blood:	n/a	n/a
42	BATF	chr2:114209720-114209940	GM12878	blood:	n/a	n/a
43	BATF	chr2:114196059-114196346	GM12878	blood:	n/a	n/a
44	BATF	chr2:114216587-114216848	GM12878	blood:	n/a	n/a
45	BATF	chr2:114188181-114188552	GM12878	blood:	n/a	n/a
46	BATF	chr2:114188569-114188750	GM12878	blood:	n/a	n/a
47	BATF	chr2:114217254-114217816	GM12878	blood:	n/a	n/a
48	BATF	chr2:114241890-114242082	GM12878	blood:	n/a	n/a
49	BATF	chr2:114174348-114174775	GM12878	blood:	n/a	n/a
50	BATF	chr2:114217280-114217821	GM12878	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114151353-114151403	HEK293	kidney:	embryo
2	chr2:114082718-114082768	SAEC	small airway:	n/a
3	chr2:114151353-114151403	HEK293	kidney:	embryo
4	chr2:114082718-114082768	SAEC	small airway:	n/a
5	chr2:114196091-114196141	T-47D	breast:	n/a
6	chr2:114082611-114082661	HCM	heart:	n/a
7	chr2:114195528-114195578	AG04450	lung:	fetal
8	chr2:114197839-114197889	NH-A	brain:	n/a
9	chr2:114082718-114082768	HL-60	blood:	n/a
10	chr2:114194541-114194591	PFSK-1	brain:	n/a
11	chr2:114195528-114195578	Caco-2	colon:	n/a
12	chr2:114164343-114164393	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:114151353-114151403	SK-N-SH_RA	brain:	n/a
14	chr2:114082611-114082661	HAEpiC	amniotic membrane:	n/a
15	chr2:114196091-114196141	HMEC	breast:	n/a
16	chr2:114194645-114194695	HUVEC	blood vessel:	n/a
17	chr2:114196058-114196108	HRE	kidney:	n/a
18	chr2:114252811-114252861	NH-A	brain:	n/a
19	chr2:114197839-114197889	HMEC	breast:	n/a
20	chr2:114196091-114196141	MCF10A-Er-Src	breast:	n/a
21	chr2:114164343-114164393	BE2_C	brain:	n/a
22	chr2:114163184-114163234	Hela-S3	cervix:	n/a
23	chr2:114194645-114194695	ProgFib	skin:	n/a
24	chr2:114164343-114164393	GM12891	blood:	n/a
25	chr2:114195528-114195578	HRCEpiC	kidney:	n/a
26	chr2:114196091-114196141	Hepatocyte	liver:	n/a
27	chr2:114163184-114163234	K562	blood:	n/a
28	chr2:114196091-114196141	HCM	heart:	n/a
29	chr2:114194541-114194591	SAEC	small airway:	n/a
30	chr2:114082718-114082768	SK-N-SH	brain:	n/a
31	chr2:114164343-114164393	Hela-S3	cervix:	n/a
32	chr2:114196058-114196108	ECC-1	luminal epithelium:	n/a
33	chr2:114196091-114196141	NB4	blood:	n/a
34	chr2:114082718-114082768	PFSK-1	brain:	n/a
35	chr2:114194541-114194591	HRE	kidney:	n/a
36	chr2:114206313-114206363	A549	lung:	n/a
37	chr2:114164343-114164393	AoSMC	blood vessel:	n/a
38	chr2:114197839-114197889	HRPEpiC	eye:	n/a
39	chr2:114164343-114164393	MCF-7	breast:	n/a
40	chr2:114206313-114206363	IMR90	lung:	fetal
41	chr2:114206313-114206363	HepG2	liver:	n/a
42	chr2:114151353-114151403	Caco-2	colon:	n/a
43	chr2:114196058-114196108	GM19239	blood:	n/a
44	chr2:114196058-114196108	HMEC	breast:	n/a
45	chr2:114163184-114163234	NB4	blood:	n/a
46	chr2:114197839-114197889	GM12878	blood:	n/a
47	chr2:114082611-114082661	T-47D	breast:	n/a
48	chr2:114163184-114163234	NH-A	brain:	n/a
49	chr2:114194541-114194591	HCM	heart:	n/a
50	chr2:114206313-114206363	HCM	heart:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114067489..114069342-chr2:114085282..114087156,2	MCF-7	breast:
2	chr14:96000768..96001608-chr2:114082065..114082796,2	HCT-116	colon:
3	chr2:114127277..114131238-chr2:114131557..114134448,3	K562	blood:
4	chr2:114010394..114011259-chr2:114127840..114128840,2	MCF-7	breast:
5	chr2:114006461..114007910-chr2:114147631..114148371,4	K562	blood:
6	chr2:114081798..114083531-chr2:114086995..114089661,2	K562	blood:
7	chr2:114087006..114091652-chr2:114092667..114098276,5	MCF-7	breast:
8	chr2:114081925..114084093-chr2:114086383..114088538,3	MCF-7	breast:
9	chr2:114006796..114007421-chr2:114127816..114128725,5	K562	blood:
10	chr2:113894600..113895171-chr2:114147816..114148753,2	MCF-7	breast:
11	chr2:114081798..114083531-chr2:114086995..114089661,2	K562	blood:
12	chr2:114006433..114007490-chr2:114127813..114128753,6	MCF-7	breast:
13	chr2:113961213..113962188-chr2:114127876..114128919,5	K562	blood:
14	chr2:113837374..113837912-chr2:114127892..114128718,2	K562	blood:
15	chr2:96406055..96406842-chr2:114139694..114140465,2	MCF-7	breast:
16	chr2:114085306..114088063-chr2:114124693..114126212,2	MCF-7	breast:
17	chr2:113988656..113991624-chr2:114097575..114099389,2	K562	blood:
18	chr2:114087006..114091652-chr2:114092667..114098276,5	MCF-7	breast:
19	chr2:113961230..113961845-chr2:114127857..114128433,2	MCF-7	breast:
20	chr12:808962..809943-chr2:114147779..114148497,2	MCF-7	breast:
21	chr2:113958498..113959276-chr2:114147736..114148311,2	K562	blood:
22	chr2:114127277..114131238-chr2:114131557..114134448,3	K562	blood:
23	chr2:114081925..114084093-chr2:114086383..114088538,3	MCF-7	breast:
24	chr2:113895658..113897096-chr2:114147534..114148565,6	K562	blood:
25	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:
26	chr2:114006491..114007402-chr2:114127850..114128740,6	MCF-7	breast:
27	chr2:114140085..114141972-chr2:114145675..114147776,2	K562	blood:
28	chr2:113952635..113954838-chr2:114132062..114134620,2	K562	blood:
29	chr2:113961603..113962131-chr2:114147652..114148320,2	K562	blood:
30	chr2:114040686..114041186-chr2:114127813..114128575,2	MCF-7	breast:
31	chr2:114140085..114141972-chr2:114145675..114147776,2	K562	blood:
32	chr2:113837351..113838104-chr2:114147540..114148341,3	K562	blood:
33	chr2:113962501..113963279-chr2:114127874..114128718,2	K562	blood:
34	chr2:114159767..114162349-chr2:114163621..114165460,2	MCF-7	breast:
35	chr2:114085306..114088063-chr2:114124693..114126212,2	MCF-7	breast:
36	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
37	chr2:114012941..114014608-chr2:114128232..114129740,2	MCF-7	breast:
38	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:
39	chr2:113961183..113962044-chr2:114147703..114148314,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC016745.1-3	chr2:114189481-114189719	expReg_chr2_8632_-
2	lnc-CBWD2-3	chr2:114082765-114083130	NONHSAT073777
3	lnc-AC016745.1-5	chr2:114184831-114185141	expReg_chr2_8625_-
4	lnc-CBWD2-2	chr2:114190177-114193619	ENSG00000272563.1
5	lnc-AC016745.1-4	chr2:114186646-114186941	expReg_chr2_8628_-
6	lnc-CBWD2-1	chr2:114182072-114182152	ENSG00000234997.1
7	lnc-CBWD2-3	chr2:114086256-114086354	NONHSAT073777
8	lnc-CBWD2-1	chr2:114182475-114182901	ENSG00000234997.1

No data

Variant related genes	Relation type
ENSG00000238091	TF binding region
CBWD2	TF binding region
ENSG00000272563	TF binding region
FOXD4L1	TF binding region
ENSG00000234997	TF binding region
IGKV1OR2-108	TF binding region
ENSG00000238091	CpG island
CBWD2	CpG island
ENSG00000272563	CpG island
FOXD4L1	CpG island
ENSG00000234997	CpG island
IGKV1OR2-108	CpG island
ENSG00000189223	chromatin interactions
ENSG00000231292	chromatin interactions
ENSG00000125637	chromatin interactions
ENSG00000247092	chromatin interactions
ENSG00000182512	chromatin interactions

Extended variants
information (count: 5238 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:5238 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542413880	chr2:114075034-114075035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138781765	chr2:114075042-114075043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575945089	chr2:114075064-114075065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561148481	chr2:114075065-114075066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544570061	chr2:114075082-114075083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556138573	chr2:114075083-114075084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564844669	chr2:114075088-114075089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532744229	chr2:114075197-114075198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540232282	chr2:114075204-114075205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142765187	chr2:114075215-114075216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35917655	chr2:114075241-114075242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574822513	chr2:114075242-114075243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185772614	chr2:114075257-114075258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10496449	chr2:114075268-114075269	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568694331	chr2:114075321-114075322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574322346	chr2:114075452-114075453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531440529	chr2:114075493-114075494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551341507	chr2:114075494-114075495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186606257	chr2:114075535-114075536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539419240	chr2:114075536-114075537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62158165	chr2:114075562-114075563	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566899948	chr2:114075600-114075601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191460949	chr2:114075609-114075610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555938846	chr2:114075620-114075621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575905089	chr2:114075670-114075671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544792824	chr2:114075673-114075674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13035667	chr2:114075676-114075677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13035675	chr2:114075678-114075679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532191542	chr2:114075679-114075680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184134453	chr2:114075718-114075719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369349161	chr2:114075868-114075869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147370166	chr2:114075873-114075874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373196658	chr2:114075883-114075884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559694998	chr2:114075896-114075897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35913167	chr2:114075929-114075930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573333920	chr2:114075958-114075959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551999761	chr2:114075986-114075987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562249026	chr2:114075999-114076000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188853033	chr2:114076027-114076028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551572152	chr2:114076032-114076033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181521653	chr2:114076036-114076037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373297112	chr2:114076067-114076068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185296238	chr2:114076070-114076071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547409366	chr2:114076093-114076094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566864836	chr2:114076173-114076174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535899075	chr2:114076183-114076184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549451619	chr2:114076193-114076194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569381370	chr2:114076202-114076203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370674363	chr2:114076227-114076228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527522370	chr2:114076251-114076252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	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
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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1430 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114064600-114082000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:114072400-114080800	Weak transcription	NHEK	skin
3	chr2:114074200-114080400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:114074200-114080800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:114074200-114081000	Weak transcription	HMEC	breast
6	chr2:114074400-114081600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:114075000-114075600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:114075200-114075800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:114077200-114079400	Weak transcription	Esophagus	oesophagus
10	chr2:114079400-114079600	Enhancers	Esophagus	oesophagus
11	chr2:114079600-114079800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:114079600-114081800	Weak transcription	Esophagus	oesophagus
13	chr2:114079800-114080400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:114080200-114080400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:114080200-114080400	Enhancers	Fetal Intestine Small	intestine
16	chr2:114080400-114081000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:114080400-114081600	Weak transcription	Fetal Intestine Small	intestine
18	chr2:114080400-114082000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:114080600-114081200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:114080600-114081800	Weak transcription	HSMMtube	muscle
21	chr2:114080600-114082000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:114080600-114082000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:114080600-114082000	Enhancers	A549	lung
24	chr2:114080600-114082200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:114080600-114082200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:114080800-114081600	Enhancers	Osteobl	bone
27	chr2:114080800-114081800	Enhancers	NHEK	skin
28	chr2:114080800-114082000	Enhancers	Fetal Brain Male	brain
29	chr2:114080800-114082200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:114081000-114082000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:114081000-114082000	Enhancers	Fetal Lung	lung
32	chr2:114081000-114082200	Enhancers	Fetal Intestine Large	intestine
33	chr2:114081000-114082200	Enhancers	HMEC	breast
34	chr2:114081200-114081600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:114081200-114081800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr2:114081200-114081800	Enhancers	NH-A	brain
37	chr2:114081200-114082000	Enhancers	Hela-S3	cervix
38	chr2:114081200-114082600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:114081400-114082000	Enhancers	Fetal Muscle Trunk	muscle
40	chr2:114081600-114081800	Enhancers	Fetal Brain Female	brain
41	chr2:114081600-114081800	Active TSS	Osteobl	bone
42	chr2:114081600-114082000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:114081600-114082000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr2:114081600-114082000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr2:114081600-114082000	Enhancers	Duodenum Mucosa	Duodenum
46	chr2:114081600-114082000	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr2:114081600-114082000	Enhancers	Fetal Stomach	stomach
48	chr2:114081600-114082000	Bivalent Enhancer	HepG2	liver
49	chr2:114081600-114082000	Enhancers	NHDF-Ad	bronchial
50	chr2:114081600-114082200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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