Variant report

Variant	nsv877229
Chromosome Location	chr3:102415127-102649650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:877)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:102433789-102434329	GM12878	blood:	n/a	n/a
2	BACH1	chr3:102648843-102648847	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:102433864-102434252	GM12878	blood:	n/a	chr3:102434009-102434020
4	BATF	chr3:102433856-102434213	GM12878	blood:	n/a	chr3:102434009-102434020
5	BCL11A	chr3:102433900-102434146	GM12878	blood:	n/a	chr3:102434012-102434021
6	BHLHE40	chr3:102422725-102422866	GM12878	blood:	n/a	n/a
7	CBX3	chr3:102433895-102434298	HCT-116	colon:	n/a	n/a
8	CBX3	chr3:102645276-102645646	HCT-116	colon:	n/a	n/a
9	CCNT2	chr3:102592280-102592455	K562	blood:	n/a	n/a
10	CEBPB	chr3:102428665-102428945	IMR90	lung:	n/a	chr3:102428795-102428808 chr3:102428795-102428806
11	CEBPB	chr3:102452913-102453375	ECC-1	luminal epithelium:	n/a	chr3:102453202-102453213
12	CEBPB	chr3:102475636-102475943	A549	lung:	n/a	chr3:102475781-102475792
13	CEBPB	chr3:102433751-102434315	HCT-116	colon:	n/a	chr3:102434071-102434083
14	CEBPB	chr3:102615745-102616028	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:102476762-102477185	HepG2	liver:	n/a	chr3:102476939-102476950
16	CEBPB	chr3:102546996-102547302	Hela-S3	cervix:	n/a	chr3:102547136-102547147 chr3:102547150-102547161
17	CEBPB	chr3:102580907-102581127	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:102444860-102445167	IMR90	lung:	n/a	chr3:102444885-102444897 chr3:102444997-102445008
19	CEBPB	chr3:102444830-102445154	HepG2	liver:	n/a	chr3:102444885-102444897 chr3:102444997-102445008
20	CEBPB	chr3:102475613-102475945	Hela-S3	cervix:	n/a	chr3:102475781-102475792
21	CEBPB	chr3:102453071-102453323	H1-hESC	embryonic stem cell:	n/a	chr3:102453202-102453213
22	CEBPB	chr3:102444867-102445137	A549	lung:	n/a	chr3:102444885-102444897 chr3:102444997-102445008
23	CEBPB	chr3:102475598-102475934	IMR90	lung:	n/a	chr3:102475781-102475792
24	CEBPB	chr3:102570426-102570698	A549	lung:	n/a	chr3:102570542-102570553
25	CEBPB	chr3:102506169-102506329	A549	lung:	n/a	n/a
26	CEBPB	chr3:102475608-102475964	HepG2	liver:	n/a	chr3:102475781-102475792
27	CEBPB	chr3:102452955-102453352	A549	lung:	n/a	chr3:102453202-102453213
28	CEBPB	chr3:102428627-102428945	HepG2	liver:	n/a	chr3:102428795-102428808 chr3:102428795-102428806
29	CEBPB	chr3:102433672-102434373	HCT-116	colon:	n/a	chr3:102434071-102434083
30	CEBPB	chr3:102476759-102477129	IMR90	lung:	n/a	chr3:102476939-102476950
31	CEBPB	chr3:102570410-102570681	Hela-S3	cervix:	n/a	chr3:102570542-102570553
32	CEBPB	chr3:102476803-102477037	H1-hESC	embryonic stem cell:	n/a	chr3:102476939-102476950
33	CEBPB	chr3:102506368-102506401	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:102491824-102492038	A549	lung:	n/a	n/a
35	CEBPB	chr3:102433925-102434214	A549	lung:	n/a	chr3:102434071-102434083
36	CEBPB	chr3:102509685-102509952	IMR90	lung:	n/a	n/a
37	CEBPB	chr3:102476791-102477082	Hela-S3	cervix:	n/a	chr3:102476939-102476950
38	CEBPB	chr3:102452678-102453419	Hela-S3	cervix:	n/a	chr3:102453202-102453213
39	CEBPB	chr3:102475622-102475965	H1-hESC	embryonic stem cell:	n/a	chr3:102475781-102475792
40	CEBPB	chr3:102615769-102615969	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:102453036-102453392	HepG2	liver:	n/a	chr3:102453202-102453213
42	CEBPB	chr3:102453029-102453385	A549	lung:	n/a	chr3:102453202-102453213
43	CEBPB	chr3:102580890-102581090	A549	lung:	n/a	n/a
44	CEBPB	chr3:102546983-102547284	A549	lung:	n/a	chr3:102547136-102547147 chr3:102547150-102547161
45	CEBPB	chr3:102506236-102506316	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:102604626-102604906	HepG2	liver:	n/a	chr3:102604766-102604777
47	CEBPB	chr3:102614513-102614802	HepG2	liver:	n/a	chr3:102614668-102614681 chr3:102614669-102614680
48	CEBPB	chr3:102546985-102547314	IMR90	lung:	n/a	chr3:102547136-102547147 chr3:102547150-102547161
49	CEBPB	chr3:102453031-102453389	IMR90	lung:	n/a	chr3:102453202-102453213
50	CEBPB	chr3:102546992-102547331	HepG2	liver:	n/a	chr3:102547136-102547147 chr3:102547150-102547161

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102452667-102452717	HL-60	blood:	n/a
2	chr3:102452667-102452717	PrEC	prostate:	n/a
3	chr3:102452667-102452717	SKMC	muscle:	n/a
4	chr3:102452667-102452717	GM12891	blood:	n/a
5	chr3:102452667-102452717	AG10803	skin:	n/a
6	chr3:102452667-102452717	Hela-S3	cervix:	n/a
7	chr3:102452667-102452717	NHBE	bronchial:	n/a
8	chr3:102452667-102452717	HUVEC	blood vessel:	n/a
9	chr3:102452667-102452717	NB4	blood:	n/a
10	chr3:102452667-102452717	ProgFib	skin:	n/a
11	chr3:102452667-102452717	AG04449	skin:	fetal
12	chr3:102452667-102452717	ovcar-3	ovarian:	n/a
13	chr3:102452667-102452717	HAEpiC	amniotic membrane:	n/a
14	chr3:102452667-102452717	HCT-116	colon:	n/a
15	chr3:102452667-102452717	Hepatocyte	liver:	n/a
16	chr3:102452667-102452717	MCF-7	breast:	n/a
17	chr3:102452667-102452717	PFSK-1	brain:	n/a
18	chr3:102452667-102452717	HNPCEpiC	eye:	n/a
19	chr3:102452667-102452717	U87	brain:	n/a
20	chr3:102452667-102452717	HCPEpiC	choroid plexus:	n/a
21	chr3:102452667-102452717	MCF10A-Er-Src	breast:	n/a
22	chr3:102452667-102452717	K562	blood:	n/a
23	chr3:102452667-102452717	SK-N-MC	brain:	n/a
24	chr3:102452667-102452717	GM12892	blood:	n/a
25	chr3:102452667-102452717	HepG2	liver:	n/a
26	chr3:102452667-102452717	BJ	skin:	n/a
27	chr3:102452667-102452717	HCM	heart:	n/a
28	chr3:102452667-102452717	HIPEpiC	eye:	n/a
29	chr3:102452667-102452717	SAEC	small airway:	n/a
30	chr3:102452667-102452717	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:102452667-102452717	BE2_C	brain:	n/a
32	chr3:102452667-102452717	RPTEC	kidney:	n/a
33	chr3:102452667-102452717	AG04450	lung:	fetal
34	chr3:102452667-102452717	AG09319	gingival:	n/a
35	chr3:102452667-102452717	Caco-2	colon:	n/a
36	chr3:102452667-102452717	HRCEpiC	kidney:	n/a
37	chr3:102452667-102452717	NT2-D1	testis:	n/a
38	chr3:102452667-102452717	HEK293	kidney:	embryo
39	chr3:102452667-102452717	NH-A	brain:	n/a
40	chr3:102452667-102452717	T-47D	breast:	n/a
41	chr3:102452667-102452717	NHDF-neo	bronchial:	n/a
42	chr3:102452667-102452717	H1-hESC	embryonic stem cell:	embryo
43	chr3:102452667-102452717	Jurkat	blood:	n/a
44	chr3:102452667-102452717	AG09309	skin:	n/a
45	chr3:102452667-102452717	HMEC	breast:	n/a
46	chr3:102452667-102452717	PANC-1	pancreas:	n/a
47	chr3:102452667-102452717	SK-N-SH	brain:	n/a
48	chr3:102452667-102452717	GM19239	blood:	n/a
49	chr3:102452667-102452717	GM12878	blood:	n/a
50	chr3:102452667-102452717	GM06990	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:102426713..102428233-chr3:161131598..161134258,2	MCF-7	breast:
2	chr17:57917124..57920044-chr3:102426713..102428447,2	MCF-7	breast:
3	chr12:56546032..56548424-chr3:102426713..102428233,2	MCF-7	breast:
4	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
5	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
6	chr3:102426713..102428233-chr9:94668915..94670633,2	K562	blood:
7	chr20:56269510..56272225-chr3:102426713..102428233,3	MCF-7	breast:
8	chr3:102392117..102393057-chr3:102459325..102460566,3	MCF-7	breast:
9	chr3:102391655..102393123-chr3:102459418..102460722,10	MCF-7	breast:
10	chr3:101954266..101954823-chr3:102459665..102460276,2	MCF-7	breast:
11	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
12	chr3:102464455..102465347-chr3:103014445..103015094,2	MCF-7	breast:
13	chr12:122459732..122460381-chr3:102427713..102428233,2	MCF-7	breast:
14	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:
15	chr3:102391603..102393690-chr3:102431669..102434137,2	MCF-7	breast:
16	chr10:6242657..6245501-chr3:102426733..102428233,2	MCF-7	breast:
17	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:
18	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
19	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
20	chr17:58677371..58678089-chr3:102427713..102428213,2	MCF-7	breast:
21	chr3:102189575..102190143-chr3:102459670..102460629,2	MCF-7	breast:
22	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
23	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
24	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
25	chr3:101954215..101955159-chr3:102459734..102460417,3	MCF-7	breast:
26	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
27	chr17:57914812..57915374-chr3:102427713..102428233,2	MCF-7	breast:
28	chr11:118778943..118781778-chr3:102426713..102428213,2	MCF-7	breast:
29	chr17:56708753..56709302-chr3:102427713..102428213,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZPLD1-4	chr3:102644557-102644725	NONHSAT090938
2	lnc-ZPLD1-1	chr3:102429679-102429722	NONHSAT090932
3	lnc-ZPLD1-1	chr3:102446237-102446410	NONHSAT090933
4	lnc-ZPLD1-1	chr3:102446238-102446423	NONHSAT090932
5	lnc-ZPLD1-1	chr3:102444626-102444901	NONHSAT090932
6	lnc-ZPLD1-2	chr3:102636251-102636282	XLOC_002743
7	lnc-ZPLD1-1	chr3:102444625-102444901	XLOC_002742
8	lnc-ZPLD1-1	chr3:102446238-102446410	XLOC_002742
9	lnc-ZPLD1-4	chr3:102644557-102644725	FPKM1_group_21624_transcript_1
10	lnc-ZPLD1-1	chr3:102444624-102444901	NONHSAT090933

No data

Variant related genes	Relation type
RNU6-461P	TF binding region
RNU6-461P	CpG island
ENSG00000170836	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000196465	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000241754	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000264211	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000110987	chromatin interactions
ARHGAP12	miRNA target sites

Extended variants
information (count: 2855 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2855 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11720453	chr3:102415127-102415128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530730403	chr3:102415152-102415153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541062306	chr3:102415172-102415173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371620460	chr3:102415176-102415177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561385506	chr3:102415177-102415178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558922141	chr3:102415214-102415215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530332905	chr3:102415219-102415220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548435909	chr3:102415233-102415234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531616673	chr3:102415319-102415320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188952005	chr3:102415336-102415337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192114377	chr3:102415398-102415399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371579478	chr3:102415449-102415450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148203873	chr3:102415454-102415455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56863685	chr3:102415486-102415487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200294483	chr3:102415488-102415489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570956695	chr3:102415498-102415499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147385846	chr3:102415500-102415501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74551561	chr3:102415564-102415565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547017837	chr3:102415728-102415729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139647062	chr3:102415730-102415731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536559701	chr3:102415754-102415755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554870133	chr3:102415776-102415777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569944042	chr3:102415799-102415800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537285538	chr3:102415803-102415804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551248579	chr3:102415839-102415840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184208606	chr3:102415875-102415876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143592153	chr3:102415897-102415898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150568535	chr3:102415929-102415930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112478175	chr3:102415979-102415980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368720920	chr3:102416057-102416058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374799761	chr3:102416072-102416073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574063531	chr3:102416085-102416086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188892689	chr3:102416092-102416093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563664651	chr3:102416121-102416122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191860123	chr3:102416134-102416135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527480629	chr3:102416141-102416142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149453981	chr3:102416156-102416157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548810129	chr3:102416193-102416194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546416345	chr3:102416261-102416262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564519561	chr3:102416267-102416268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528589371	chr3:102416295-102416296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547074996	chr3:102416318-102416319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141585336	chr3:102416323-102416324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35726263	chr3:102416351-102416352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56896657	chr3:102416354-102416355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568481122	chr3:102416397-102416398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529334223	chr3:102416404-102416405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562102995	chr3:102416411-102416412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376908487	chr3:102416412-102416413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550978547	chr3:102416415-102416416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102415000-102416800	Weak transcription	Fetal Heart	heart
2	chr3:102416400-102416600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:102416800-102417000	Enhancers	Fetal Heart	heart
4	chr3:102417000-102417200	Flanking Active TSS	Fetal Heart	heart
5	chr3:102417200-102417400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:102417200-102417400	ZNF genes & repeats	Left Ventricle	heart
7	chr3:102417200-102420000	Enhancers	Fetal Heart	heart
8	chr3:102417400-102419000	Weak transcription	Left Ventricle	heart
9	chr3:102420000-102421200	Weak transcription	Fetal Heart	heart
10	chr3:102421200-102423600	Enhancers	Fetal Heart	heart
11	chr3:102421800-102422000	Enhancers	Left Ventricle	heart
12	chr3:102428400-102429400	Enhancers	Brain Germinal Matrix	brain
13	chr3:102432000-102432200	Enhancers	GM12878-XiMat	blood
14	chr3:102432400-102433400	Weak transcription	GM12878-XiMat	blood
15	chr3:102433400-102433600	Enhancers	GM12878-XiMat	blood
16	chr3:102433400-102434400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:102433600-102433800	Flanking Active TSS	GM12878-XiMat	blood
18	chr3:102433600-102434000	Enhancers	Fetal Lung	lung
19	chr3:102433600-102434200	Enhancers	Fetal Kidney	kidney
20	chr3:102433600-102434400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:102433600-102434400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr3:102433600-102434400	Enhancers	NH-A	brain
23	chr3:102433600-102434600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:102433600-102434600	Enhancers	HMEC	breast
25	chr3:102433600-102434600	Enhancers	NHEK	skin
26	chr3:102433800-102434000	Enhancers	GM12878-XiMat	blood
27	chr3:102433800-102434400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:102434000-102434200	Flanking Active TSS	GM12878-XiMat	blood
29	chr3:102434000-102434400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:102434000-102434400	Enhancers	Hela-S3	cervix
31	chr3:102434200-102434400	Active TSS	GM12878-XiMat	blood
32	chr3:102434400-102434600	Flanking Active TSS	GM12878-XiMat	blood
33	chr3:102435600-102436200	Enhancers	Fetal Thymus	thymus
34	chr3:102436200-102436800	Enhancers	Fetal Heart	heart
35	chr3:102436800-102440600	Weak transcription	Fetal Heart	heart
36	chr3:102440600-102441600	Enhancers	Fetal Heart	heart
37	chr3:102446400-102446600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:102446600-102452200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:102447800-102448200	Enhancers	Ovary	ovary
40	chr3:102448000-102448400	Enhancers	Fetal Heart	heart
41	chr3:102448400-102452200	Weak transcription	Fetal Heart	heart
42	chr3:102452000-102453200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr3:102452000-102453800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:102452000-102454200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:102452000-102454400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:102452000-102456200	Enhancers	Fetal Lung	lung
47	chr3:102452200-102453600	Enhancers	NH-A	brain
48	chr3:102452200-102453800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:102452200-102454000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:102452200-102457600	Enhancers	Fetal Heart	heart

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