Variant report

Variant	nsv834776
Chromosome Location	chr3:102351486-102532042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:999)
CpG islands
(count:183)
Chromatin interactive
region (count:32)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:102392377-102392677	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:102389996-102390294	HepG2	liver:	n/a	n/a
3	ATF2	chr3:102433789-102434329	GM12878	blood:	n/a	n/a
4	ATF2	chr3:102407030-102407386	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:102406889-102407383	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:102433856-102434213	GM12878	blood:	n/a	chr3:102434009-102434020
7	BATF	chr3:102433864-102434252	GM12878	blood:	n/a	chr3:102434009-102434020
8	BCL11A	chr3:102407072-102407277	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr3:102407054-102407384	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr3:102433900-102434146	GM12878	blood:	n/a	chr3:102434012-102434021
11	BCLAF1	chr3:102392318-102392743	GM12878	blood:	n/a	chr3:102392461-102392470
12	BCLAF1	chr3:102392360-102392720	GM12878	blood:	n/a	chr3:102392461-102392470
13	BHLHE40	chr3:102422725-102422866	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:102392374-102392692	GM12878	blood:	n/a	n/a
15	BRCA1	chr3:102392547-102392568	HepG2	liver:	n/a	n/a
16	BRCA1	chr3:102392399-102392703	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr3:102433895-102434298	HCT-116	colon:	n/a	n/a
18	CEBPB	chr3:102475636-102475943	A549	lung:	n/a	chr3:102475781-102475792
19	CEBPB	chr3:102453071-102453323	H1-hESC	embryonic stem cell:	n/a	chr3:102453202-102453213
20	CEBPB	chr3:102453029-102453385	A549	lung:	n/a	chr3:102453202-102453213
21	CEBPB	chr3:102506236-102506316	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:102366863-102366980	A549	lung:	n/a	n/a
23	CEBPB	chr3:102444830-102445154	HepG2	liver:	n/a	chr3:102444885-102444897 chr3:102444997-102445008
24	CEBPB	chr3:102433751-102434315	HCT-116	colon:	n/a	chr3:102434071-102434083
25	CEBPB	chr3:102475622-102475965	H1-hESC	embryonic stem cell:	n/a	chr3:102475781-102475792
26	CEBPB	chr3:102433672-102434373	HCT-116	colon:	n/a	chr3:102434071-102434083
27	CEBPB	chr3:102476691-102477111	A549	lung:	n/a	chr3:102476939-102476950
28	CEBPB	chr3:102433925-102434214	A549	lung:	n/a	chr3:102434071-102434083
29	CEBPB	chr3:102428665-102428945	IMR90	lung:	n/a	chr3:102428795-102428808 chr3:102428795-102428806
30	CEBPB	chr3:102491824-102492038	A549	lung:	n/a	n/a
31	CEBPB	chr3:102452970-102453402	ECC-1	luminal epithelium:	n/a	chr3:102453202-102453213
32	CEBPB	chr3:102506368-102506401	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr3:102476791-102477082	Hela-S3	cervix:	n/a	chr3:102476939-102476950
34	CEBPB	chr3:102475608-102475964	HepG2	liver:	n/a	chr3:102475781-102475792
35	CEBPB	chr3:102369586-102369668	A549	lung:	n/a	n/a
36	CEBPB	chr3:102452678-102453419	Hela-S3	cervix:	n/a	chr3:102453202-102453213
37	CEBPB	chr3:102523312-102523449	A549	lung:	n/a	n/a
38	CEBPB	chr3:102452913-102453375	ECC-1	luminal epithelium:	n/a	chr3:102453202-102453213
39	CEBPB	chr3:102453031-102453389	IMR90	lung:	n/a	chr3:102453202-102453213
40	CEBPB	chr3:102475613-102475945	Hela-S3	cervix:	n/a	chr3:102475781-102475792
41	CEBPB	chr3:102506169-102506329	A549	lung:	n/a	n/a
42	CEBPB	chr3:102475598-102475934	IMR90	lung:	n/a	chr3:102475781-102475792
43	CEBPB	chr3:102444867-102445137	A549	lung:	n/a	chr3:102444885-102444897 chr3:102444997-102445008
44	CEBPB	chr3:102453036-102453392	HepG2	liver:	n/a	chr3:102453202-102453213
45	CEBPB	chr3:102433864-102434493	Hela-S3	cervix:	n/a	chr3:102434071-102434083
46	CEBPB	chr3:102452955-102453352	A549	lung:	n/a	chr3:102453202-102453213
47	CEBPB	chr3:102509685-102509952	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:102428627-102428945	HepG2	liver:	n/a	chr3:102428795-102428808 chr3:102428795-102428806
49	CEBPB	chr3:102476759-102477129	IMR90	lung:	n/a	chr3:102476939-102476950
50	CEBPB	chr3:102476762-102477185	HepG2	liver:	n/a	chr3:102476939-102476950

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102452667-102452717	IMR90	lung:	fetal
2	chr3:102392777-102392827	HIPEpiC	eye:	n/a
3	chr3:102399370-102399420	PANC-1	pancreas:	n/a
4	chr3:102392777-102392827	NHDF-neo	bronchial:	n/a
5	chr3:102452667-102452717	GM12878	blood:	n/a
6	chr3:102399370-102399420	HRCEpiC	kidney:	n/a
7	chr3:102452667-102452717	HCM	heart:	n/a
8	chr3:102392777-102392827	SK-N-MC	brain:	n/a
9	chr3:102399370-102399420	BJ	skin:	n/a
10	chr3:102452667-102452717	AoSMC	blood vessel:	n/a
11	chr3:102399370-102399420	HepG2	liver:	n/a
12	chr3:102452667-102452717	HRE	kidney:	n/a
13	chr3:102399370-102399420	AoSMC	blood vessel:	n/a
14	chr3:102392777-102392827	HUVEC	blood vessel:	n/a
15	chr3:102452667-102452717	HCPEpiC	choroid plexus:	n/a
16	chr3:102452667-102452717	HEK293	kidney:	embryo
17	chr3:102392777-102392827	Jurkat	blood:	n/a
18	chr3:102399370-102399420	SK-N-SH_RA	brain:	n/a
19	chr3:102452667-102452717	PrEC	prostate:	n/a
20	chr3:102392777-102392827	RPTEC	kidney:	n/a
21	chr3:102399370-102399420	H1-hESC	embryonic stem cell:	embryo
22	chr3:102399370-102399420	ECC-1	luminal epithelium:	n/a
23	chr3:102452667-102452717	ECC-1	luminal epithelium:	n/a
24	chr3:102392777-102392827	A549	lung:	n/a
25	chr3:102392777-102392827	HEK293	kidney:	embryo
26	chr3:102452667-102452717	HEEpiC	esophagus:	n/a
27	chr3:102392777-102392827	H1-hESC	embryonic stem cell:	embryo
28	chr3:102392777-102392827	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:102392777-102392827	IMR90	lung:	fetal
30	chr3:102452667-102452717	HepG2	liver:	n/a
31	chr3:102392777-102392827	AG04449	skin:	fetal
32	chr3:102392777-102392827	MCF10A-Er-Src	breast:	n/a
33	chr3:102392777-102392827	NB4	blood:	n/a
34	chr3:102452667-102452717	PANC-1	pancreas:	n/a
35	chr3:102452667-102452717	HL-60	blood:	n/a
36	chr3:102399370-102399420	T-47D	breast:	n/a
37	chr3:102452667-102452717	HNPCEpiC	eye:	n/a
38	chr3:102452667-102452717	MCF-7	breast:	n/a
39	chr3:102392777-102392827	ovcar-3	ovarian:	n/a
40	chr3:102399370-102399420	HCM	heart:	n/a
41	chr3:102399370-102399420	HCT-116	colon:	n/a
42	chr3:102392777-102392827	HCF	heart:	n/a
43	chr3:102452667-102452717	CMK	blood:	n/a
44	chr3:102392777-102392827	GM12878	blood:	n/a
45	chr3:102392777-102392827	HRCEpiC	kidney:	n/a
46	chr3:102392777-102392827	CMK	blood:	n/a
47	chr3:102452667-102452717	AG04449	skin:	fetal
48	chr3:102452667-102452717	GM12891	blood:	n/a
49	chr3:102399370-102399420	MCF-7	breast:	n/a
50	chr3:102452667-102452717	RPTEC	kidney:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:102189575..102190143-chr3:102459670..102460629,2	MCF-7	breast:
2	chr3:102426713..102428233-chr3:161131598..161134258,2	MCF-7	breast:
3	chr3:102392117..102393057-chr3:102459325..102460566,3	MCF-7	breast:
4	chr3:102464455..102465347-chr3:103014445..103015094,2	MCF-7	breast:
5	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
6	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
7	chr17:56708753..56709302-chr3:102427713..102428213,2	MCF-7	breast:
8	chr12:56546032..56548424-chr3:102426713..102428233,2	MCF-7	breast:
9	chr17:58677371..58678089-chr3:102427713..102428213,2	MCF-7	breast:
10	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
11	chr20:56269510..56272225-chr3:102426713..102428233,3	MCF-7	breast:
12	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
13	chr3:102391655..102393123-chr3:102459418..102460722,10	MCF-7	breast:
14	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
15	chr11:118778943..118781778-chr3:102426713..102428213,2	MCF-7	breast:
16	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
17	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
18	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
19	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
20	chr10:6242657..6245501-chr3:102426733..102428233,2	MCF-7	breast:
21	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
22	chr3:101954266..101954823-chr3:102459665..102460276,2	MCF-7	breast:
23	chr12:122459732..122460381-chr3:102427713..102428233,2	MCF-7	breast:
24	chr3:102426713..102428233-chr9:94668915..94670633,2	K562	blood:
25	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
26	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
27	chr3:101954215..101955159-chr3:102459734..102460417,3	MCF-7	breast:
28	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
29	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
30	chr17:57917124..57920044-chr3:102426713..102428447,2	MCF-7	breast:
31	chr17:57914812..57915374-chr3:102427713..102428233,2	MCF-7	breast:
32	chr3:102391603..102393690-chr3:102431669..102434137,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
2	lnc-RPL24-2	chr3:102392598-102392802	XLOC_003194
3	lnc-ZPLD1-1	chr3:102444625-102444901	XLOC_002742
4	lnc-ZPLD1-1	chr3:102446237-102446410	NONHSAT090933
5	lnc-RPL24-2	chr3:102392598-102392850	XLOC_003194
6	lnc-RPL24-2	chr3:102379501-102379812	XLOC_003194
7	lnc-ZPLD1-1	chr3:102429679-102429722	NONHSAT090932
8	lnc-ZPLD1-1	chr3:102446238-102446410	XLOC_002742
9	lnc-RPL24-2	chr3:102382007-102382267	XLOC_003194
10	lnc-ZPLD1-1	chr3:102444624-102444901	NONHSAT090933
11	lnc-ZPLD1-1	chr3:102446238-102446423	NONHSAT090932
12	lnc-RPL24-2	chr3:102392598-102392757	XLOC_003194
13	lnc-ZPLD1-1	chr3:102444626-102444901	NONHSAT090932
14	lnc-RPL24-2	chr3:102382143-102382168	XLOC_003194
15	lnc-RPL24-2	chr3:102387891-102388106	XLOC_003194
16	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
17	lnc-RPL24-2	chr3:102383382-102384456	XLOC_003194

No data

Variant related genes	Relation type
RNU6-461P	TF binding region
ENSG00000241754	TF binding region
RNU6-461P	CpG island
ENSG00000241754	CpG island
ENSG00000241754	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000196465	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000264211	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000110987	chromatin interactions
ENSG00000212195	chromatin interactions
FAM122A	miRNA target sites
FAM122B	miRNA target sites

Extended variants
information (count: 3723 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3723 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188547718	chr3:102351505-102351506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11915586	chr3:102351541-102351542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200602053	chr3:102351588-102351589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs68032122	chr3:102351589-102351590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377127287	chr3:102351591-102351592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201221631	chr3:102351592-102351593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569402253	chr3:102351595-102351596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539562740	chr3:102351600-102351601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557863550	chr3:102351622-102351623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371273560	chr3:102351624-102351625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200359681	chr3:102351625-102351626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538317823	chr3:102351632-102351633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567984669	chr3:102351633-102351634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574649339	chr3:102351634-102351635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149489553	chr3:102351645-102351646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556894233	chr3:102351672-102351673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575430476	chr3:102351701-102351702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191517590	chr3:102351707-102351708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564216686	chr3:102351714-102351715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183603980	chr3:102351745-102351746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201433156	chr3:102351771-102351772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143986118	chr3:102351818-102351819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189498685	chr3:102351822-102351823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538648509	chr3:102351844-102351845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529581709	chr3:102351870-102351871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551219207	chr3:102351941-102351942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13322672	chr3:102351983-102351984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558081729	chr3:102352006-102352007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573006103	chr3:102352007-102352008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148666137	chr3:102352038-102352039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1284723	chr3:102352039-102352040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548991119	chr3:102352047-102352048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143472056	chr3:102352051-102352052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537836476	chr3:102352101-102352102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146286228	chr3:102352111-102352112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575446431	chr3:102352112-102352113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372478531	chr3:102352133-102352134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377035459	chr3:102352134-102352135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573961861	chr3:102352135-102352136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs397791703	chr3:102352143-102352144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369344695	chr3:102352144-102352145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539684775	chr3:102352278-102352279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557943046	chr3:102352284-102352285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182050738	chr3:102352290-102352291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187375097	chr3:102352296-102352297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561543253	chr3:102352332-102352333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73134053	chr3:102352352-102352353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60357682	chr3:102352358-102352359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563240676	chr3:102352362-102352363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533408589	chr3:102352369-102352370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102350400-102352400	Weak transcription	Pancreas	Pancrea
2	chr3:102367400-102367600	Enhancers	Stomach Mucosa	stomach
3	chr3:102367600-102368000	Active TSS	Stomach Mucosa	stomach
4	chr3:102368000-102369000	Weak transcription	Stomach Mucosa	stomach
5	chr3:102369000-102369400	Enhancers	Stomach Mucosa	stomach
6	chr3:102374600-102375600	Enhancers	Stomach Mucosa	stomach
7	chr3:102379400-102383400	Enhancers	Liver	Liver
8	chr3:102381200-102381400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr3:102383400-102389000	Weak transcription	Liver	Liver
10	chr3:102385800-102387400	Enhancers	Stomach Mucosa	stomach
11	chr3:102387200-102387600	Enhancers	Fetal Muscle Leg	muscle
12	chr3:102387400-102389400	Weak transcription	Stomach Mucosa	stomach
13	chr3:102389000-102392200	Enhancers	Liver	Liver
14	chr3:102389400-102390000	Enhancers	Stomach Mucosa	stomach
15	chr3:102389600-102390400	Enhancers	Fetal Intestine Small	intestine
16	chr3:102389800-102390400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:102389800-102390400	Enhancers	HepG2	liver
18	chr3:102389800-102392000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr3:102390000-102392200	Weak transcription	Stomach Mucosa	stomach
20	chr3:102390400-102392600	Weak transcription	HepG2	liver
21	chr3:102390800-102391000	Enhancers	Brain Anterior Caudate	brain
22	chr3:102391000-102392600	Weak transcription	Brain Anterior Caudate	brain
23	chr3:102391200-102391400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:102391200-102394800	Enhancers	Fetal Heart	heart
25	chr3:102392000-102392200	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr3:102392200-102392400	Enhancers	Fetal Lung	lung
27	chr3:102392200-102392400	Enhancers	Stomach Mucosa	stomach
28	chr3:102392200-102392600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr3:102392200-102392800	Flanking Active TSS	Liver	Liver
30	chr3:102392200-102392800	Active TSS	Right Atrium	heart
31	chr3:102392200-102393000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr3:102392200-102393000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:102392200-102393000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:102392200-102393000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr3:102392200-102393000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr3:102392200-102393000	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr3:102392200-102393000	Enhancers	Fetal Stomach	stomach
38	chr3:102392400-102392600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:102392400-102392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:102392400-102392600	Enhancers	Brain Germinal Matrix	brain
41	chr3:102392400-102392600	Enhancers	Fetal Kidney	kidney
42	chr3:102392400-102392600	Active TSS	Ovary	ovary
43	chr3:102392400-102392600	Active TSS	NH-A	brain
44	chr3:102392400-102392800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr3:102392400-102392800	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr3:102392400-102392800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:102392400-102392800	Flanking Active TSS	Fetal Lung	lung
48	chr3:102392400-102392800	Active TSS	Fetal Muscle Trunk	muscle
49	chr3:102392400-102392800	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr3:102392400-102392800	Active TSS	Stomach Mucosa	stomach

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