Variant report

Variant	nsv1002402
Chromosome Location	chr3:101277-236728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:310)
CpG islands
(count:184)
Chromatin interactive
region (count:10)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:104725-105176	HepG2	liver:	n/a	n/a
2	ATF1	chr3:128118-128267	K562	blood:	n/a	n/a
3	BACH1	chr3:165624-165661	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:166561-166841	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
5	BATF	chr3:166548-166773	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
6	BHLHE40	chr3:152996-153196	A549	lung:	n/a	n/a
7	BHLHE40	chr3:150637-150664	A549	lung:	n/a	n/a
8	CCNT2	chr3:210502-210583	K562	blood:	n/a	n/a
9	CEBPB	chr3:157527-157838	HepG2	liver:	n/a	chr3:157561-157572 chr3:157692-157703
10	CEBPB	chr3:219203-219482	A549	lung:	n/a	n/a
11	CEBPB	chr3:130437-130508	A549	lung:	n/a	n/a
12	CEBPB	chr3:169853-170053	A549	lung:	n/a	n/a
13	CEBPB	chr3:216135-216492	A549	lung:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
14	CEBPB	chr3:215306-215533	K562	blood:	n/a	chr3:215398-215409 chr3:215397-215410
15	CEBPB	chr3:104930-105426	HepG2	liver:	n/a	chr3:105311-105324
16	CEBPB	chr3:111396-111753	Hela-S3	cervix:	n/a	chr3:111564-111575 chr3:111563-111574
17	CEBPB	chr3:211035-211283	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:216138-216415	Hela-S3	cervix:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
19	CEBPB	chr3:137940-138307	HepG2	liver:	n/a	chr3:138113-138124 chr3:138111-138128
20	CEBPB	chr3:215234-215549	HepG2	liver:	n/a	chr3:215398-215409 chr3:215397-215410
21	CEBPB	chr3:216151-216444	HepG2	liver:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
22	CEBPB	chr3:111431-111722	HepG2	liver:	n/a	chr3:111564-111575 chr3:111563-111574
23	CEBPB	chr3:110019-110065	A549	lung:	n/a	n/a
24	CEBPB	chr3:219216-219513	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:162469-162671	A549	lung:	n/a	n/a
26	CEBPB	chr3:215340-215517	A549	lung:	n/a	chr3:215398-215409 chr3:215397-215410
27	CEBPB	chr3:157534-157826	IMR90	lung:	n/a	chr3:157561-157572 chr3:157692-157703
28	CHD1	chr3:195466-195490	GM12878	blood:	n/a	n/a
29	CHD2	chr3:105065-105090	HepG2	liver:	n/a	n/a
30	CHD2	chr3:166635-166663	GM12878	blood:	n/a	n/a
31	CTCF	chr3:108296-108341	GM19239	blood:	n/a	n/a
32	CTCF	chr3:108220-108370	HepG2	liver:	n/a	n/a
33	CTCF	chr3:108140-108290	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:197800-197950	HEK293	kidney:	n/a	n/a
35	CTCF	chr3:108241-108351	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:197860-198010	RPTEC	kidney:	n/a	n/a
37	CTCF	chr3:108292-108360	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr3:108256-108265	GM20000	blood:	n/a	n/a
39	CTCF	chr3:108309-108354	GM12878	blood:	n/a	n/a
40	CTCF	chr3:178275-178321	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:197800-197950	HAc	cerebellar:	n/a	n/a
42	CTCF	chr3:108226-108422	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:165953-165988	GM13976	blood:	n/a	n/a
44	CTCF	chr3:178240-178390	HepG2	liver:	n/a	n/a
45	CTCF	chr3:197740-197890	GM12878	blood:	n/a	n/a
46	CTCF	chr3:178200-178350	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:197840-197990	GM06990	blood:	n/a	n/a
48	CTCF	chr3:128198-128255	GM19239	blood:	n/a	n/a
49	CTCF	chr3:108246-108372	HepG2	liver:	n/a	n/a
50	CTCF	chr3:197780-197930	GM12866	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:114243-114293	CMK	blood:	n/a
2	chr3:114243-114293	CMK	blood:	n/a
3	chr3:236078-236128	Caco-2	colon:	n/a
4	chr3:236078-236128	Hepatocyte	liver:	n/a
5	chr3:153242-153292	HIPEpiC	eye:	n/a
6	chr3:114243-114293	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:153242-153292	LNCaP	prostate:	n/a
8	chr3:153242-153292	U87	brain:	n/a
9	chr3:236078-236128	BJ	skin:	n/a
10	chr3:114243-114293	HRCEpiC	kidney:	n/a
11	chr3:114243-114293	NHBE	bronchial:	n/a
12	chr3:114243-114293	PrEC	prostate:	n/a
13	chr3:153242-153292	PFSK-1	brain:	n/a
14	chr3:153242-153292	HCPEpiC	choroid plexus:	n/a
15	chr3:236078-236128	ProgFib	skin:	n/a
16	chr3:236078-236128	ECC-1	luminal epithelium:	n/a
17	chr3:153242-153292	HEK293	kidney:	embryo
18	chr3:153242-153292	HMEC	breast:	n/a
19	chr3:236078-236128	GM12891	blood:	n/a
20	chr3:236078-236128	Hela-S3	cervix:	n/a
21	chr3:114243-114293	NB4	blood:	n/a
22	chr3:236078-236128	AG10803	skin:	n/a
23	chr3:236078-236128	T-47D	breast:	n/a
24	chr3:153242-153292	HUVEC	blood vessel:	n/a
25	chr3:114243-114293	AG04449	skin:	fetal
26	chr3:114243-114293	SKMC	muscle:	n/a
27	chr3:153242-153292	HCM	heart:	n/a
28	chr3:236078-236128	HCPEpiC	choroid plexus:	n/a
29	chr3:236078-236128	HEEpiC	esophagus:	n/a
30	chr3:153242-153292	SK-N-MC	brain:	n/a
31	chr3:153242-153292	AG09319	gingival:	n/a
32	chr3:114243-114293	ovcar-3	ovarian:	n/a
33	chr3:236078-236128	IMR90	lung:	fetal
34	chr3:153242-153292	BE2_C	brain:	n/a
35	chr3:236078-236128	HRE	kidney:	n/a
36	chr3:114243-114293	HepG2	liver:	n/a
37	chr3:114243-114293	AoSMC	blood vessel:	n/a
38	chr3:153242-153292	PANC-1	pancreas:	n/a
39	chr3:114243-114293	BE2_C	brain:	n/a
40	chr3:114243-114293	GM12878	blood:	n/a
41	chr3:114243-114293	HUVEC	blood vessel:	n/a
42	chr3:236078-236128	MCF-7	breast:	n/a
43	chr3:114243-114293	HEEpiC	esophagus:	n/a
44	chr3:236078-236128	Jurkat	blood:	n/a
45	chr3:236078-236128	NT2-D1	testis:	n/a
46	chr3:114243-114293	HAEpiC	amniotic membrane:	n/a
47	chr3:114243-114293	NHDF-neo	bronchial:	n/a
48	chr3:236078-236128	HCT-116	colon:	n/a
49	chr3:153242-153292	GM12892	blood:	n/a
50	chr3:153242-153292	HepG2	liver:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
2	chr11:73160067..73160822-chr3:118894..119482,2	MCF-7	breast:
3	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
4	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
5	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
6	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
7	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
8	chr3:188824..190368-chr3:386265..388997,2	MCF-7	breast:
9	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
10	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-1	chr3:109401-109695	XLOC_002563
2	lnc-IL5RA-17	chr3:147014-147245	l_2301_chr3:147013-148034_heart
3	lnc-IL5RA-16	chr3:157540-157620	NONHSAT087554
4	lnc-IL5RA-16	chr3:153927-154143	NONHSAT087555
5	lnc-CHL1-1	chr3:111531-111980	XLOC_002563
6	lnc-IL5RA-17	chr3:147879-148034	l_2301_chr3:147013-148034_heart
7	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
8	lnc-CHL1-1	chr3:111531-111663	XLOC_002563
9	lnc-CHL1-1	chr3:109310-109695	XLOC_002563
10	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
11	lnc-CHL1-1	chr3:109310-109435	XLOC_002563
12	lnc-IL5RA-16	chr3:157540-157624	NONHSAT087555
13	lnc-IL5RA-16	chr3:172879-173007	NONHSAT087554
14	lnc-IL5RA-16	chr3:153782-154143	NONHSAT087554

No data

Variant related genes	Relation type
CHL1	TF binding region
CHL1	CpG island

Extended variants
information (count: 4297 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4297 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549185581	chr3:101280-101281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185019989	chr3:101281-101282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186673808	chr3:101286-101287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148104543	chr3:101292-101293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191495625	chr3:101302-101303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571251493	chr3:101305-101306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141905210	chr3:101328-101329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553762528	chr3:101333-101334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570688386	chr3:101382-101383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559038789	chr3:101428-101429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536524715	chr3:101434-101435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184721591	chr3:101436-101437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147233623	chr3:101464-101465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543245623	chr3:101481-101482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61124255	chr3:101521-101522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577671800	chr3:101523-101524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139049197	chr3:101536-101537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75189475	chr3:101537-101538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527656292	chr3:101585-101586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528392730	chr3:101590-101591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546958415	chr3:101604-101605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568009798	chr3:101611-101612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531978594	chr3:101625-101626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143724026	chr3:101676-101677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571328750	chr3:101696-101697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532211672	chr3:101724-101725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147225920	chr3:101780-101781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535109509	chr3:101826-101827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556993857	chr3:101860-101861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565708379	chr3:101863-101864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536240391	chr3:101881-101882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554891772	chr3:101885-101886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569851800	chr3:101892-101893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369755181	chr3:101908-101909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76682867	chr3:101944-101945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558430503	chr3:101983-101984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539172826	chr3:102062-102063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577734899	chr3:102075-102076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545124086	chr3:102076-102077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189583927	chr3:102078-102079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376536552	chr3:102090-102091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181601614	chr3:102119-102120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185141243	chr3:102133-102134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189079047	chr3:102135-102136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181816095	chr3:102146-102147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186316577	chr3:102147-102148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115290587	chr3:102168-102169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540482949	chr3:102170-102171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189547135	chr3:102182-102183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140487472	chr3:102205-102206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Ependymoma	20639864	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:95600-104600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:98000-104800	Weak transcription	Fetal Brain Male	brain
3	chr3:103600-104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:103800-104200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:104200-104400	Enhancers	Gastric	stomach
6	chr3:104400-104800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:104400-105000	Weak transcription	Gastric	stomach
8	chr3:104400-105400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:104400-105400	Enhancers	HepG2	liver
10	chr3:104400-105600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:104600-104800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:104600-104800	Enhancers	Adipose Nuclei	Adipose
13	chr3:104600-104800	Enhancers	Brain Substantia Nigra	brain
14	chr3:104600-105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:104600-105600	Enhancers	Fetal Lung	lung
16	chr3:104800-105000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:104800-105000	Active TSS	Brain Germinal Matrix	brain
18	chr3:104800-105000	Enhancers	Stomach Mucosa	stomach
19	chr3:104800-105200	Enhancers	Fetal Brain Male	brain
20	chr3:104800-105400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:104800-105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:104800-105400	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr3:104800-105400	Enhancers	Brain Angular Gyrus	brain
24	chr3:104800-105400	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr3:104800-105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:104800-105600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:104800-105600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr3:104800-105600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr3:104800-105600	Enhancers	Brain Hippocampus Middle	brain
30	chr3:104800-105600	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr3:104800-105600	Enhancers	Fetal Brain Female	brain
32	chr3:104800-105600	Enhancers	Psoas Muscle	Psoas
33	chr3:104800-105800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr3:105000-105200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:105000-105200	Enhancers	Liver	Liver
36	chr3:105000-105400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr3:105000-105400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:105000-105400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr3:105000-105400	Enhancers	Pancreas	Pancrea
40	chr3:105000-105600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr3:105000-105600	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr3:105000-105600	Enhancers	Brain Cingulate Gyrus	brain
43	chr3:105000-105600	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr3:105000-105600	Enhancers	Gastric	stomach
45	chr3:105200-105400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr3:105200-105400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:105200-105400	Flanking Active TSS	Liver	Liver
48	chr3:105200-105400	Flanking Active TSS	Fetal Brain Male	brain
49	chr3:105400-105600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:105400-105600	Enhancers	Adipose Nuclei	Adipose

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