Variant report

Variant	nsv524557
Chromosome Location	chr3:102364297-102394152
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	ARID3A	chr3:102389996-102390294	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:102392377-102392677	HepG2	liver:	n/a	n/a
3	BCLAF1	chr3:102392360-102392720	GM12878	blood:	n/a	chr3:102392461-102392470
4	BCLAF1	chr3:102392318-102392743	GM12878	blood:	n/a	chr3:102392461-102392470
5	BHLHE40	chr3:102392374-102392692	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:102392547-102392568	HepG2	liver:	n/a	n/a
7	BRCA1	chr3:102392399-102392703	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:102369586-102369668	A549	lung:	n/a	n/a
9	CEBPB	chr3:102366863-102366980	A549	lung:	n/a	n/a
10	CHD2	chr3:102392401-102392707	GM12878	blood:	n/a	n/a
11	CHD2	chr3:102392380-102392748	Hela-S3	cervix:	n/a	n/a
12	CREB1	chr3:102392406-102392703	A549	lung:	n/a	n/a
13	CTCF	chr3:102392460-102392610	HPF	lung:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
14	CTCF	chr3:102392460-102392610	GM12874	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
15	CTCF	chr3:102392331-102392707	Spleen_OC	spleen:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
16	CTCF	chr3:102392460-102392610	GM12878	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
17	CTCF	chr3:102392410-102392714	GM19238	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
18	CTCF	chr3:102392460-102392610	WERI-Rb-1	eye:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
19	CTCF	chr3:102392440-102392590	HVMF	connective:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
20	CTCF	chr3:102392460-102392610	AoAF	blood vessel:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
21	CTCF	chr3:102392460-102392610	HepG2	liver:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
22	CTCF	chr3:102392417-102392690	GM12892	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
23	CTCF	chr3:102392440-102392590	HFF	foreskin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
24	CTCF	chr3:102392440-102392590	HCM	heart:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
25	CTCF	chr3:102392340-102392490	WI-38	lung:	n/a	n/a
26	CTCF	chr3:102392460-102392610	GM12867	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
27	CTCF	chr3:102392440-102392590	GM12864	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
28	CTCF	chr3:102392460-102392610	GM12872	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
29	CTCF	chr3:102392781-102392787	A549	lung:	n/a	n/a
30	CTCF	chr3:102392187-102392316	GM10248	blood:	n/a	n/a
31	CTCF	chr3:102392398-102392658	A549	lung:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
32	CTCF	chr3:102392460-102392610	NHLF	lung:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
33	CTCF	chr3:102392380-102392530	A549	lung:	n/a	n/a
34	CTCF	chr3:102392460-102392610	GM12866	blood:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
35	CTCF	chr3:102392440-102392590	AoAF	blood vessel:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
36	CTCF	chr3:102392400-102392550	HAc	cerebellar:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
37	CTCF	chr3:102392460-102392610	BJ	skin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
38	CTCF	chr3:102392440-102392590	AG04450	lung:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
39	CTCF	chr3:102392460-102392610	HCPEpiC	choroid plexus:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
40	CTCF	chr3:102392416-102392686	Fibrobl	skin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
41	CTCF	chr3:102392500-102392650	HFF-Myc	foreskin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
42	CTCF	chr3:102392480-102392630	AG09309	skin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
43	CTCF	chr3:102392402-102392675	MCF-7	breast:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
44	CTCF	chr3:102392440-102392590	HepG2	liver:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
45	CTCF	chr3:102392480-102392630	AG04449	skin:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
46	CTCF	chr3:102392271-102392779	MCF-7	breast:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
47	CTCF	chr3:102392480-102392630	HCPEpiC	choroid plexus:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
48	CTCF	chr3:102392480-102392630	RPTEC	kidney:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
49	CTCF	chr3:102392480-102392630	HUVEC	blood vessel:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542
50	CTCF	chr3:102392412-102392824	HCT-116	colon:	n/a	chr3:102392525-102392543 chr3:102392530-102392538 chr3:102392527-102392548 chr3:102392526-102392542

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102392777-102392827	GM12891	blood:	n/a
2	chr3:102392777-102392827	GM12891	blood:	n/a
3	chr3:102392777-102392827	NB4	blood:	n/a
4	chr3:102392777-102392827	A549	lung:	n/a
5	chr3:102392777-102392827	LNCaP	prostate:	n/a
6	chr3:102392777-102392827	SK-N-SH_RA	brain:	n/a
7	chr3:102392777-102392827	HAEpiC	amniotic membrane:	n/a
8	chr3:102392777-102392827	GM12892	blood:	n/a
9	chr3:102392777-102392827	ECC-1	luminal epithelium:	n/a
10	chr3:102392777-102392827	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:102392777-102392827	SKMC	muscle:	n/a
12	chr3:102392777-102392827	BJ	skin:	n/a
13	chr3:102392777-102392827	HCF	heart:	n/a
14	chr3:102392777-102392827	HRCEpiC	kidney:	n/a
15	chr3:102392777-102392827	AG04449	skin:	fetal
16	chr3:102392777-102392827	NH-A	brain:	n/a
17	chr3:102392777-102392827	U87	brain:	n/a
18	chr3:102392777-102392827	SAEC	small airway:	n/a
19	chr3:102392777-102392827	AG10803	skin:	n/a
20	chr3:102392777-102392827	HIPEpiC	eye:	n/a
21	chr3:102392777-102392827	SK-N-SH	brain:	n/a
22	chr3:102392777-102392827	MCF-7	breast:	n/a
23	chr3:102392777-102392827	MCF10A-Er-Src	breast:	n/a
24	chr3:102392777-102392827	AG09309	skin:	n/a
25	chr3:102392777-102392827	HRPEpiC	eye:	n/a
26	chr3:102392777-102392827	HCM	heart:	n/a
27	chr3:102392777-102392827	AG04450	lung:	fetal
28	chr3:102392777-102392827	GM19239	blood:	n/a
29	chr3:102392777-102392827	Jurkat	blood:	n/a
30	chr3:102392777-102392827	H1-hESC	embryonic stem cell:	embryo
31	chr3:102392777-102392827	NHBE	bronchial:	n/a
32	chr3:102392777-102392827	NT2-D1	testis:	n/a
33	chr3:102392777-102392827	BE2_C	brain:	n/a
34	chr3:102392777-102392827	AoSMC	blood vessel:	n/a
35	chr3:102392777-102392827	Caco-2	colon:	n/a
36	chr3:102392777-102392827	PANC-1	pancreas:	n/a
37	chr3:102392777-102392827	GM12878	blood:	n/a
38	chr3:102392777-102392827	HRE	kidney:	n/a
39	chr3:102392777-102392827	ProgFib	skin:	n/a
40	chr3:102392777-102392827	HepG2	liver:	n/a
41	chr3:102392777-102392827	HCPEpiC	choroid plexus:	n/a
42	chr3:102392777-102392827	HNPCEpiC	eye:	n/a
43	chr3:102392777-102392827	HL-60	blood:	n/a
44	chr3:102392777-102392827	Hepatocyte	liver:	n/a
45	chr3:102392777-102392827	HMEC	breast:	n/a
46	chr3:102392777-102392827	NHDF-neo	bronchial:	n/a
47	chr3:102392777-102392827	CMK	blood:	n/a
48	chr3:102392777-102392827	PFSK-1	brain:	n/a
49	chr3:102392777-102392827	K562	blood:	n/a
50	chr3:102392777-102392827	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
2	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
3	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
4	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
5	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
6	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL24-2	chr3:102387891-102388106	XLOC_003194
2	lnc-RPL24-2	chr3:102383382-102384456	XLOC_003194
3	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
4	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
5	lnc-RPL24-2	chr3:102392598-102392850	XLOC_003194
6	lnc-RPL24-2	chr3:102382143-102382168	XLOC_003194
7	lnc-RPL24-2	chr3:102379501-102379812	XLOC_003194
8	lnc-RPL24-2	chr3:102382007-102382267	XLOC_003194
9	lnc-RPL24-2	chr3:102392598-102392757	XLOC_003194
10	lnc-RPL24-2	chr3:102392598-102392802	XLOC_003194

Variant related genes	Relation type
ENSG00000241754	TF binding region
ENSG00000241754	CpG island
FAM122B	miRNA target sites
FAM122A	miRNA target sites

Extended variants
information (count: 672 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537516879	chr3:102367439-102367440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150865985	chr3:102367515-102367516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182111750	chr3:102367518-102367519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531574814	chr3:102367520-102367521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534699907	chr3:102367529-102367530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148996263	chr3:102367537-102367538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557417840	chr3:102367550-102367551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571961791	chr3:102367680-102367681	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs542434554	chr3:102367718-102367719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs560713928	chr3:102367732-102367733	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575815139	chr3:102367738-102367739	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187771029	chr3:102367748-102367749	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs139364863	chr3:102367771-102367772	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532177159	chr3:102367781-102367782	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143053873	chr3:102367782-102367783	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs560095050	chr3:102367855-102367856	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs575598759	chr3:102367906-102367907	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546134751	chr3:102367915-102367916	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs1464116	chr3:102367926-102367927	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548817493	chr3:102368024-102368025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73863965	chr3:102368049-102368050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532415938	chr3:102368057-102368058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139072636	chr3:102368068-102368069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192340358	chr3:102368069-102368070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570816933	chr3:102368101-102368102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374407268	chr3:102368122-102368123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80249453	chr3:102368139-102368140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144007917	chr3:102368164-102368165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536173080	chr3:102368209-102368210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554419201	chr3:102368293-102368294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576230718	chr3:102368314-102368315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35848274	chr3:102368328-102368329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397775723	chr3:102368338-102368339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71798770	chr3:102368339-102368340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200368148	chr3:102368340-102368341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115947237	chr3:102368366-102368367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72946922	chr3:102368410-102368411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs57757391	chr3:102368455-102368456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs56163111	chr3:102368500-102368501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183209073	chr3:102368504-102368505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529699085	chr3:102368530-102368531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548927631	chr3:102368536-102368537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563968342	chr3:102368538-102368539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531143775	chr3:102368557-102368558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368333817	chr3:102368594-102368595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570946159	chr3:102368597-102368598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188839752	chr3:102368638-102368639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546672113	chr3:102368650-102368651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148625357	chr3:102368737-102368738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535451761	chr3:102368775-102368776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102367400-102367600	Enhancers	Stomach Mucosa	stomach
2	chr3:102367600-102368000	Active TSS	Stomach Mucosa	stomach
3	chr3:102368000-102369000	Weak transcription	Stomach Mucosa	stomach
4	chr3:102369000-102369400	Enhancers	Stomach Mucosa	stomach
5	chr3:102374600-102375600	Enhancers	Stomach Mucosa	stomach
6	chr3:102379400-102383400	Enhancers	Liver	Liver
7	chr3:102381200-102381400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:102383400-102389000	Weak transcription	Liver	Liver
9	chr3:102385800-102387400	Enhancers	Stomach Mucosa	stomach
10	chr3:102387200-102387600	Enhancers	Fetal Muscle Leg	muscle
11	chr3:102387400-102389400	Weak transcription	Stomach Mucosa	stomach
12	chr3:102389000-102392200	Enhancers	Liver	Liver
13	chr3:102389400-102390000	Enhancers	Stomach Mucosa	stomach
14	chr3:102389600-102390400	Enhancers	Fetal Intestine Small	intestine
15	chr3:102389800-102390400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:102389800-102390400	Enhancers	HepG2	liver
17	chr3:102389800-102392000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr3:102390000-102392200	Weak transcription	Stomach Mucosa	stomach
19	chr3:102390400-102392600	Weak transcription	HepG2	liver
20	chr3:102390800-102391000	Enhancers	Brain Anterior Caudate	brain
21	chr3:102391000-102392600	Weak transcription	Brain Anterior Caudate	brain
22	chr3:102391200-102391400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:102391200-102394800	Enhancers	Fetal Heart	heart
24	chr3:102392000-102392200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr3:102392200-102392400	Enhancers	Fetal Lung	lung
26	chr3:102392200-102392400	Enhancers	Stomach Mucosa	stomach
27	chr3:102392200-102392600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:102392200-102392800	Flanking Active TSS	Liver	Liver
29	chr3:102392200-102392800	Active TSS	Right Atrium	heart
30	chr3:102392200-102393000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:102392200-102393000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:102392200-102393000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:102392200-102393000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:102392200-102393000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr3:102392200-102393000	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr3:102392200-102393000	Enhancers	Fetal Stomach	stomach
37	chr3:102392400-102392600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr3:102392400-102392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr3:102392400-102392600	Enhancers	Brain Germinal Matrix	brain
40	chr3:102392400-102392600	Enhancers	Fetal Kidney	kidney
41	chr3:102392400-102392600	Active TSS	Ovary	ovary
42	chr3:102392400-102392600	Active TSS	NH-A	brain
43	chr3:102392400-102392800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr3:102392400-102392800	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr3:102392400-102392800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:102392400-102392800	Flanking Active TSS	Fetal Lung	lung
47	chr3:102392400-102392800	Active TSS	Fetal Muscle Trunk	muscle
48	chr3:102392400-102392800	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr3:102392400-102392800	Active TSS	Stomach Mucosa	stomach
50	chr3:102392400-102392800	Active TSS	Hela-S3	cervix

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