Variant report

Variant	nsv536785
Chromosome Location	chr3:162703918-162894644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:755)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr3:162717002-162717061	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr3:162774855-162774871	HepG2	liver:	n/a	n/a
3	BRCA1	chr3:162774683-162774995	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr3:162774587-162774998	MCF-7	breast:	n/a	n/a
5	CEBPB	chr3:162815267-162815649	MCF-7	breast:	n/a	chr3:162815435-162815446
6	CEBPB	chr3:162815287-162815558	IMR90	lung:	n/a	chr3:162815435-162815446
7	CEBPB	chr3:162774571-162774995	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:162815303-162815572	A549	lung:	n/a	chr3:162815435-162815446
9	CEBPB	chr3:162729383-162729666	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:162729092-162729733	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:162893798-162893837	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:162774594-162775003	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:162856075-162856324	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:162729220-162729874	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:162789480-162789977	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:162815262-162815596	HepG2	liver:	n/a	chr3:162815435-162815446
17	CEBPB	chr3:162773968-162774176	HepG2	liver:	n/a	chr3:162774022-162774033
18	CEBPB	chr3:162729522-162729600	A549	lung:	n/a	n/a
19	CEBPB	chr3:162711790-162712125	HepG2	liver:	n/a	chr3:162711927-162711938
20	CEBPB	chr3:162774590-162774941	A549	lung:	n/a	n/a
21	CEBPB	chr3:162729049-162729851	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:162711839-162712097	IMR90	lung:	n/a	chr3:162711927-162711938
23	CTCF	chr3:162774760-162774910	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr3:162774760-162774910	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr3:162774805-162774914	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr3:162774780-162774930	HRE	kidney:	n/a	n/a
27	CTCF	chr3:162774759-162774975	K562	blood:	n/a	n/a
28	CTCF	chr3:162775080-162775230	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:162774800-162774950	HFF	foreskin:	n/a	n/a
30	CTCF	chr3:162774800-162774950	GM12878	blood:	n/a	n/a
31	CTCF	chr3:162774780-162774930	AG09319	gingival:	n/a	n/a
32	CTCF	chr3:162774780-162774930	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr3:162774727-162774920	ECC-1	luminal epithelium:	n/a	n/a
34	CTCF	chr3:162774744-162774992	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr3:162774340-162774490	NHEK	skin:	n/a	n/a
36	CTCF	chr3:162791855-162791872	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:162774594-162775152	HCT-116	colon:	n/a	n/a
38	CTCF	chr3:162791861-162791922	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:162760915-162761248	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:162774488-162775188	SK-N-SH	brain:	n/a	n/a
41	CTCF	chr3:162761040-162761190	GM12868	blood:	n/a	n/a
42	CTCF	chr3:162760938-162761184	Gliobla	brain:	n/a	n/a
43	CTCF	chr3:162774800-162774950	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr3:162774780-162774930	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:162774765-162774934	A549	lung:	n/a	n/a
46	CTCF	chr3:162884766-162884837	Lung_OC	lung:	n/a	n/a
47	CTCF	chr3:162774820-162774970	GM12868	blood:	n/a	n/a
48	CTCF	chr3:162774700-162774850	RPTEC	kidney:	n/a	n/a
49	CTCF	chr3:162760980-162761130	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr3:162774780-162774930	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162705337-162705387	HCM	heart:	n/a
2	chr3:162705337-162705387	GM06990	blood:	n/a
3	chr3:162705203-162705253	HL-60	blood:	n/a
4	chr3:162705427-162705477	U87	brain:	n/a
5	chr3:162705203-162705253	HCF	heart:	n/a
6	chr3:162705427-162705477	Caco-2	colon:	n/a
7	chr3:162705427-162705477	AG09319	gingival:	n/a
8	chr3:162705203-162705253	HCM	heart:	n/a
9	chr3:162705337-162705387	AG09309	skin:	n/a
10	chr3:162705203-162705253	AG04450	lung:	fetal
11	chr3:162705203-162705253	Jurkat	blood:	n/a
12	chr3:162705203-162705253	HCT-116	colon:	n/a
13	chr3:162705337-162705387	HCT-116	colon:	n/a
14	chr3:162705203-162705253	H1-hESC	embryonic stem cell:	embryo
15	chr3:162705337-162705387	MCF-7	breast:	n/a
16	chr3:162705203-162705253	ProgFib	skin:	n/a
17	chr3:162705203-162705253	NB4	blood:	n/a
18	chr3:162705427-162705477	BJ	skin:	n/a
19	chr3:162705203-162705253	NHBE	bronchial:	n/a
20	chr3:162705427-162705477	AG04450	lung:	fetal
21	chr3:162705337-162705387	GM12891	blood:	n/a
22	chr3:162705337-162705387	NHDF-neo	bronchial:	n/a
23	chr3:162705427-162705477	NT2-D1	testis:	n/a
24	chr3:162705337-162705387	CMK	blood:	n/a
25	chr3:162705337-162705387	ProgFib	skin:	n/a
26	chr3:162705427-162705477	HCPEpiC	choroid plexus:	n/a
27	chr3:162705203-162705253	HUVEC	blood vessel:	n/a
28	chr3:162705427-162705477	Hepatocyte	liver:	n/a
29	chr3:162705337-162705387	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:162705337-162705387	NT2-D1	testis:	n/a
31	chr3:162705427-162705477	AoSMC	blood vessel:	n/a
32	chr3:162705337-162705387	Hepatocyte	liver:	n/a
33	chr3:162705427-162705477	H1-hESC	embryonic stem cell:	embryo
34	chr3:162705203-162705253	PrEC	prostate:	n/a
35	chr3:162705427-162705477	SK-N-SH_RA	brain:	n/a
36	chr3:162705203-162705253	HEEpiC	esophagus:	n/a
37	chr3:162705337-162705387	HEK293	kidney:	embryo
38	chr3:162705203-162705253	GM12878	blood:	n/a
39	chr3:162705203-162705253	IMR90	lung:	fetal
40	chr3:162705203-162705253	AG09309	skin:	n/a
41	chr3:162705203-162705253	HepG2	liver:	n/a
42	chr3:162705203-162705253	HMEC	breast:	n/a
43	chr3:162705427-162705477	HUVEC	blood vessel:	n/a
44	chr3:162705203-162705253	HRCEpiC	kidney:	n/a
45	chr3:162705203-162705253	HCPEpiC	choroid plexus:	n/a
46	chr3:162705337-162705387	SK-N-MC	brain:	n/a
47	chr3:162705337-162705387	T-47D	breast:	n/a
48	chr3:162705337-162705387	HCF	heart:	n/a
49	chr3:162705427-162705477	HMEC	breast:	n/a
50	chr3:162705203-162705253	BJ	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:162754967..162757825-chr3:162758379..162760616,2	MCF-7	breast:
2	chr3:162755966..162757761-chr3:162760804..162762764,2	MCF-7	breast:
3	chr3:162781747..162783965-chr3:162788037..162790015,2	MCF-7	breast:
4	chr3:156892021..156894345-chr3:162787273..162789725,2	MCF-7	breast:
5	chr3:162755966..162757761-chr3:162760804..162762764,2	MCF-7	breast:
6	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:
7	chr2:174218936..174220527-chr3:162835384..162836884,2	K562	blood:
8	chr3:162781747..162783965-chr3:162788037..162790015,2	MCF-7	breast:
9	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:
10	chr3:162774415..162775478-chr3:163207241..163208645,5	MCF-7	breast:
11	chr3:162821263..162822976-chr3:162826872..162828945,2	MCF-7	breast:
12	chr3:162776529..162777484-chr3:163340191..163340771,2	MCF-7	breast:
13	chr3:162754967..162757825-chr3:162758379..162760616,2	MCF-7	breast:
14	chr14:60627662..60628534-chr3:162740219..162740719,2	MCF-7	breast:
15	chr3:162821263..162822976-chr3:162826872..162828945,2	MCF-7	breast:
16	chr3:162829065..162831690-chr3:162831998..162834078,2	MCF-7	breast:
17	chr3:162003324..162004086-chr3:162760294..162761113,2	MCF-7	breast:
18	chr3:162494680..162495563-chr3:162760633..162761552,3	MCF-7	breast:
19	chr3:162774576..162775267-chr3:162991199..162992106,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-2	chr3:162744184-162744286	ENSG00000241168.1
2	lnc-SI-4	chr3:162845711-162845859	ENSG00000241369
3	lnc-OTOL1-2	chr3:162744184-162744286	NONHSAT093026
4	lnc-OTOL1-9	chr3:162833217-162833974	NONHSAT093027

No data

Variant related genes	Relation type
ENSG00000244571	TF binding region
ENSG00000241168	TF binding region
ENSG00000244571	CpG island
ENSG00000241168	CpG island
ENSG00000244571	chromatin interactions
ENSG00000243176	chromatin interactions
ENSG00000144354	chromatin interactions

Extended variants
information (count: 2991 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2991 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558529623	chr3:162703969-162703970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs578253117	chr3:162704005-162704006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs9682941	chr3:162704006-162704007	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs10513598	chr3:162704020-162704021	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs573920167	chr3:162704059-162704060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs543140583	chr3:162704060-162704061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs16855266	chr3:162704091-162704092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs548945065	chr3:162704155-162704156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs543990664	chr3:162704176-162704177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs142098298	chr3:162704197-162704198	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs567546882	chr3:162704217-162704218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs9852069	chr3:162704223-162704224	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs13318277	chr3:162704254-162704255	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546459883	chr3:162704277-162704278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs9869731	chr3:162704325-162704326	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs368975171	chr3:162704348-162704349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs547952870	chr3:162704399-162704400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs528862083	chr3:162704435-162704436	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs549110621	chr3:162704466-162704467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs190791434	chr3:162704487-162704488	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs537900521	chr3:162704509-162704510	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs61223757	chr3:162704534-162704535	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs61149205	chr3:162704535-162704536	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs558388769	chr3:162704573-162704574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs571845023	chr3:162704582-162704583	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs534514260	chr3:162704593-162704594	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs538269484	chr3:162704605-162704606	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs574005099	chr3:162704633-162704634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs542650859	chr3:162704710-162704711	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs369342010	chr3:162704723-162704724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs200758161	chr3:162704725-162704726	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs556656102	chr3:162704726-162704727	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs568896017	chr3:162704749-162704750	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs540473085	chr3:162704767-162704768	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs576466315	chr3:162704785-162704786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs537643076	chr3:162704789-162704790	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs561479601	chr3:162704816-162704817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9870585	chr3:162704823-162704824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs563961512	chr3:162704826-162704827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184032871	chr3:162704856-162704857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114550445	chr3:162704867-162704868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560185819	chr3:162704877-162704878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73027121	chr3:162704880-162704881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548713593	chr3:162704888-162704889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145927422	chr3:162704891-162704892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192336125	chr3:162704904-162704905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551469089	chr3:162704911-162704912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372518000	chr3:162704912-162704913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73027123	chr3:162704913-162704914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs377044915	chr3:162704927-162704928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162703200-162704800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr3:162704800-162707800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:162710600-162710800	Enhancers	Dnd41	blood
4	chr3:162710800-162711000	Weak transcription	Dnd41	blood
5	chr3:162711000-162713600	ZNF genes & repeats	Dnd41	blood
6	chr3:162713600-162714400	Weak transcription	Dnd41	blood
7	chr3:162714400-162714800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:162714400-162715200	Enhancers	Dnd41	blood
9	chr3:162715200-162716400	Flanking Active TSS	Dnd41	blood
10	chr3:162715400-162716000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:162715400-162716200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:162715400-162716200	Enhancers	Colon Smooth Muscle	Colon
13	chr3:162715400-162716200	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr3:162715600-162715800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:162715600-162716000	Active TSS	Adipose Nuclei	Adipose
16	chr3:162715600-162716000	Active TSS	Aorta	Aorta
17	chr3:162715600-162716000	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr3:162715600-162716000	Active TSS	Stomach Smooth Muscle	stomach
19	chr3:162715600-162716200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:162715600-162716200	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr3:162715600-162716800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:162715800-162716000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:162715800-162716600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:162715800-162716600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:162716000-162716200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:162716000-162716200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:162716200-162716400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:162716200-162716600	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr3:162716400-162718000	Enhancers	Dnd41	blood
30	chr3:162724800-162725600	Enhancers	Dnd41	blood
31	chr3:162735400-162745200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:162735600-162736400	Enhancers	Fetal Heart	heart
33	chr3:162736600-162737400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr3:162741000-162765600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr3:162745200-162745600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr3:162745600-162746000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:162752200-162752800	Enhancers	Dnd41	blood
38	chr3:162752800-162753200	Weak transcription	Dnd41	blood
39	chr3:162753200-162753400	Enhancers	Dnd41	blood
40	chr3:162753400-162756000	Weak transcription	Dnd41	blood
41	chr3:162756000-162756800	Enhancers	Dnd41	blood
42	chr3:162756800-162757200	Weak transcription	Dnd41	blood
43	chr3:162757200-162758000	Enhancers	Dnd41	blood
44	chr3:162762000-162763200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:162762600-162763400	Enhancers	Adipose Nuclei	Adipose
46	chr3:162762600-162764000	Enhancers	Dnd41	blood
47	chr3:162764000-162764400	Flanking Active TSS	Dnd41	blood
48	chr3:162764400-162765000	Enhancers	Dnd41	blood
49	chr3:162765000-162769000	Weak transcription	Dnd41	blood
50	chr3:162765600-162766000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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