Variant report

Variant	esv3350238
Chromosome Location	chr2:33849408-33979026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:33903556-33903740	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:33895782-33896011	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr2:33931333-33931739	GM12878	blood:	n/a	chr2:33931614-33931623
4	BHLHE40	chr2:33930236-33930245	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:33950219-33950224	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:33931274-33931873	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:33954808-33954914	GM12878	blood:	n/a	n/a
8	BRCA1	chr2:33895774-33895781	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr2:33890166-33890396	K562	blood:	n/a	n/a
10	CEBPB	chr2:33956627-33956689	K562	blood:	n/a	n/a
11	CEBPB	chr2:33944200-33944431	H1-hESC	embryonic stem cell:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
12	CEBPB	chr2:33933176-33933406	HepG2	liver:	n/a	chr2:33933236-33933247
13	CEBPB	chr2:33936116-33936240	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:33876705-33876938	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:33884684-33884706	HepG2	liver:	n/a	chr2:33884688-33884699
16	CEBPB	chr2:33911667-33911867	A549	lung:	n/a	n/a
17	CEBPB	chr2:33944152-33944511	A549	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
18	CEBPB	chr2:33876708-33877010	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:33911633-33911893	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:33944196-33944468	K562	blood:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
21	CEBPB	chr2:33876670-33877029	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:33933222-33933250	IMR90	lung:	n/a	chr2:33933236-33933247
23	CEBPB	chr2:33944156-33944508	HepG2	liver:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
24	CEBPB	chr2:33876672-33877000	A549	lung:	n/a	n/a
25	CEBPB	chr2:33933206-33933369	A549	lung:	n/a	chr2:33933236-33933247
26	CEBPB	chr2:33944156-33944511	IMR90	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
27	CEBPB	chr2:33944249-33944412	MCF-7	breast:	n/a	chr2:33944333-33944350 chr2:33944334-33944347 chr2:33944335-33944346
28	CHD1	chr2:33924263-33924289	GM12878	blood:	n/a	n/a
29	CHD1	chr2:33932620-33932635	GM12878	blood:	n/a	n/a
30	CHD2	chr2:33931345-33932144	GM12878	blood:	n/a	n/a
31	CTCF	chr2:33899100-33899298	Lung_OC	lung:	n/a	chr2:33899191-33899209 chr2:33899192-33899208 chr2:33899193-33899214 chr2:33899196-33899204
32	CTCF	chr2:33892020-33892170	AG09309	skin:	n/a	n/a
33	CTCF	chr2:33899020-33899170	SAEC	small airway:	n/a	n/a
34	CTCF	chr2:33895747-33895906	IMR90	lung:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796
35	CTCF	chr2:33906540-33906690	GM12873	blood:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
36	CTCF	chr2:33899140-33899290	NHEK	skin:	n/a	chr2:33899191-33899209 chr2:33899192-33899208 chr2:33899193-33899214 chr2:33899196-33899204
37	CTCF	chr2:33895740-33895890	GM12867	blood:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796
38	CTCF	chr2:33906560-33906710	HA-sp	spinal cord:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
39	CTCF	chr2:33906480-33906630	HCPEpiC	choroid plexus:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
40	CTCF	chr2:33895781-33895874	GM12892	blood:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796
41	CTCF	chr2:33906460-33906610	HCFaa	heart:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
42	CTCF	chr2:33906520-33906670	RPTEC	kidney:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
43	CTCF	chr2:33895720-33895870	NB4	blood:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796
44	CTCF	chr2:33906480-33906630	GM06990	blood:	n/a	chr2:33906587-33906600 chr2:33906586-33906607
45	CTCF	chr2:33895700-33895850	HEEpiC	esophagus:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796
46	CTCF	chr2:33899136-33899206	MCF-7	breast:	n/a	chr2:33899196-33899204
47	CTCF	chr2:33892050-33892216	Fibrobl	skin:	n/a	n/a
48	CTCF	chr2:33899200-33899350	HFF	foreskin:	n/a	n/a
49	CTCF	chr2:33906440-33906590	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:33895700-33895850	GM12873	blood:	n/a	chr2:33895788-33895801 chr2:33895787-33895808 chr2:33895789-33895796

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33954735-33954785	SK-N-MC	brain:	n/a
2	chr2:33929187-33929237	GM12878	blood:	n/a
3	chr2:33952509-33952559	SK-N-MC	brain:	n/a
4	chr2:33954735-33954785	SK-N-MC	brain:	n/a
5	chr2:33929187-33929237	GM12878	blood:	n/a
6	chr2:33952509-33952559	SK-N-MC	brain:	n/a
7	chr2:33948457-33948507	Hela-S3	cervix:	n/a
8	chr2:33952509-33952559	NHBE	bronchial:	n/a
9	chr2:33906282-33906332	HAEpiC	amniotic membrane:	n/a
10	chr2:33952509-33952559	RPTEC	kidney:	n/a
11	chr2:33953203-33953253	NHDF-neo	bronchial:	n/a
12	chr2:33954043-33954093	HCM	heart:	n/a
13	chr2:33953437-33953487	GM12891	blood:	n/a
14	chr2:33954735-33954785	NHDF-neo	bronchial:	n/a
15	chr2:33952423-33952473	SK-N-SH	brain:	n/a
16	chr2:33929187-33929237	Hepatocyte	liver:	n/a
17	chr2:33905480-33905530	Hepatocyte	liver:	n/a
18	chr2:33954347-33954397	SK-N-SH_RA	brain:	n/a
19	chr2:33952509-33952559	HAEpiC	amniotic membrane:	n/a
20	chr2:33952673-33952723	HIPEpiC	eye:	n/a
21	chr2:33952488-33952538	BE2_C	brain:	n/a
22	chr2:33952509-33952559	NHDF-neo	bronchial:	n/a
23	chr2:33954735-33954785	PrEC	prostate:	n/a
24	chr2:33954043-33954093	NT2-D1	testis:	n/a
25	chr2:33952509-33952559	IMR90	lung:	fetal
26	chr2:33948457-33948507	GM12878	blood:	n/a
27	chr2:33953437-33953487	HUVEC	blood vessel:	n/a
28	chr2:33951647-33951697	AG10803	skin:	n/a
29	chr2:33906282-33906332	HL-60	blood:	n/a
30	chr2:33929187-33929237	RPTEC	kidney:	n/a
31	chr2:33948457-33948507	HCM	heart:	n/a
32	chr2:33953195-33953245	NH-A	brain:	n/a
33	chr2:33906282-33906332	BJ	skin:	n/a
34	chr2:33954043-33954093	HRCEpiC	kidney:	n/a
35	chr2:33953203-33953253	SK-N-SH	brain:	n/a
36	chr2:33948457-33948507	GM06990	blood:	n/a
37	chr2:33952488-33952538	Jurkat	blood:	n/a
38	chr2:33905480-33905530	GM06990	blood:	n/a
39	chr2:33953195-33953245	ProgFib	skin:	n/a
40	chr2:33953370-33953420	SK-N-SH_RA	brain:	n/a
41	chr2:33953195-33953245	GM06990	blood:	n/a
42	chr2:33906282-33906332	SK-N-SH	brain:	n/a
43	chr2:33953437-33953487	HNPCEpiC	eye:	n/a
44	chr2:33952423-33952473	GM06990	blood:	n/a
45	chr2:33952673-33952723	MCF-7	breast:	n/a
46	chr2:33951647-33951697	SK-N-SH_RA	brain:	n/a
47	chr2:33906282-33906332	K562	blood:	n/a
48	chr2:33954043-33954093	SK-N-SH_RA	brain:	n/a
49	chr2:33954347-33954397	AG04449	skin:	fetal
50	chr2:33953203-33953253	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:33973736..33977470-chr2:33981372..33984191,3	K562	blood:
2	chr2:33866715..33868482-chr2:33873359..33875488,2	MCF-7	breast:
3	chr2:33906087..33906631-chr2:34321375..34322022,2	MCF-7	breast:
4	chr2:33906151..33906814-chr2:34795262..34796206,5	MCF-7	breast:
5	chr2:33862671..33864955-chr2:33868719..33871401,2	K562	blood:
6	chr2:33848285..33850159-chr2:33851964..33854579,2	MCF-7	breast:
7	chr2:33869867..33872136-chr2:33872580..33874510,2	K562	blood:
8	chr2:33926109..33928802-chr2:33930360..33932286,2	K562	blood:
9	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
10	chr2:33866715..33868482-chr2:33873359..33875488,2	MCF-7	breast:
11	chr2:33848285..33850159-chr2:33851964..33854579,2	MCF-7	breast:
12	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
13	chr2:33862671..33864955-chr2:33868719..33871401,2	K562	blood:
14	chr2:33869867..33872136-chr2:33872580..33874510,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM98A-4	chr2:33947328-33947937	NONHSAT147081
2	lnc-FAM98A-4	chr2:33948350-33948577	NONHSAT147081
3	lnc-RASGRP3-1	chr2:33931975-33932020	ENSG00000203386
4	lnc-RASGRP3-1	chr2:33931953-33932020	ENSG00000203386

Variant related genes	Relation type
HNRNPA1P61	TF binding region
ENSG00000203386	TF binding region
MYADML	TF binding region
HNRNPA1P61	CpG island
ENSG00000203386	CpG island
MYADML	CpG island
ENSG00000203386	chromatin interactions

Extended variants
information (count: 3647 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3647 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386644609	chr2:33849456-33849457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs60913270	chr2:33849467-33849468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs58006815	chr2:33849469-33849470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569546368	chr2:33849497-33849498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370418058	chr2:33849523-33849524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114062239	chr2:33849541-33849542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138852751	chr2:33849555-33849556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs59809293	chr2:33849581-33849582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs534779735	chr2:33849647-33849648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554481862	chr2:33849657-33849658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182574110	chr2:33849671-33849672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187557541	chr2:33849703-33849704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115873744	chr2:33849709-33849710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575990118	chr2:33849733-33849734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142148465	chr2:33849840-33849841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145756054	chr2:33849876-33849877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192015838	chr2:33849910-33849911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369973645	chr2:33849930-33849931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548105519	chr2:33849937-33849938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561301562	chr2:33849947-33849948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34790188	chr2:33849948-33849949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72542305	chr2:33849956-33849957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397868648	chr2:33849957-33849958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370179054	chr2:33849958-33849959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530363984	chr2:33849967-33849968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148177902	chr2:33850052-33850053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569776361	chr2:33850087-33850088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114544893	chr2:33850093-33850094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552221749	chr2:33850103-33850104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565943785	chr2:33850104-33850105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59291573	chr2:33850118-33850119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57801405	chr2:33850127-33850128	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs568154481	chr2:33850129-33850130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141373661	chr2:33850131-33850132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565318679	chr2:33850134-33850135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142007840	chr2:33850161-33850162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183329112	chr2:33850174-33850175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150516886	chr2:33850180-33850181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs118153963	chr2:33850189-33850190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189237740	chr2:33850348-33850349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139454635	chr2:33850350-33850351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575505625	chr2:33850371-33850372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6713874	chr2:33850382-33850383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs561663754	chr2:33850395-33850396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193077068	chr2:33850435-33850436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530190714	chr2:33850470-33850471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535451153	chr2:33850487-33850488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543997945	chr2:33850495-33850496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1448562	chr2:33850500-33850501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs183641099	chr2:33850554-33850555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33845200-33859400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:33845200-33859600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:33849400-33849600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:33849400-33849800	Enhancers	Ovary	ovary
5	chr2:33849800-33850800	Weak transcription	Ovary	ovary
6	chr2:33850800-33851400	Enhancers	Ovary	ovary
7	chr2:33851400-33853400	Weak transcription	Ovary	ovary
8	chr2:33853200-33854000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr2:33853400-33853800	Enhancers	Ovary	ovary
10	chr2:33855200-33859600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr2:33856400-33856800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:33857400-33858600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:33858200-33859600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr2:33859400-33859600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr2:33859400-33859800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:33859400-33860200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr2:33859400-33860200	Enhancers	Placenta	Placenta
18	chr2:33859600-33859800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:33859600-33859800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:33859600-33859800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr2:33859800-33862000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:33860000-33862200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr2:33860400-33862800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr2:33860400-33862800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:33860600-33861600	Enhancers	Fetal Heart	heart
26	chr2:33860600-33862200	Enhancers	Primary hematopoietic stem cells	blood
27	chr2:33860600-33863200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr2:33868600-33870800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr2:33869400-33869800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:33869400-33869800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:33869800-33871000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:33869800-33878000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:33870600-33871200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:33870800-33871000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:33870800-33871200	Enhancers	Psoas Muscle	Psoas
36	chr2:33870800-33871400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:33870800-33871600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:33870800-33871600	Enhancers	Adipose Nuclei	Adipose
39	chr2:33871000-33871200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:33871200-33871600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:33879000-33880800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:33880400-33880800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:33880600-33895800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:33880800-33888600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:33885800-33886200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:33886000-33887400	Enhancers	Placenta	Placenta
47	chr2:33887800-33889000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:33888200-33888600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:33888600-33889000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr2:33888600-33889400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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