Variant report

Variant	nsv829651
Chromosome Location	chr3:105203424-105402136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1195)
CpG islands
(count:671)
Chromatin interactive
region (count:40)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1195 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:105218503-105218622	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:105237717-105238073	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:105221309-105222893	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:105375613-105375817	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:105333040-105333707	K562	blood:	n/a	n/a
6	ATF1	chr3:105333135-105333577	K562	blood:	n/a	n/a
7	ATF1	chr3:105368415-105368938	K562	blood:	n/a	n/a
8	ATF1	chr3:105365926-105366226	K562	blood:	n/a	n/a
9	ATF3	chr3:105365817-105366267	K562	blood:	n/a	n/a
10	ATF3	chr3:105365835-105366305	HCT-116	colon:	n/a	n/a
11	ATF3	chr3:105365964-105366152	K562	blood:	n/a	n/a
12	ATF3	chr3:105365812-105366303	HCT-116	colon:	n/a	n/a
13	ATF3	chr3:105365945-105366202	HepG2	liver:	n/a	n/a
14	ATF3	chr3:105365858-105366281	A549	lung:	n/a	n/a
15	BACH1	chr3:105298985-105299090	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:105242369-105242687	K562	blood:	n/a	n/a
17	BATF	chr3:105246829-105247210	GM12878	blood:	n/a	chr3:105247029-105247040
18	BATF	chr3:105287689-105287848	GM12878	blood:	n/a	n/a
19	BATF	chr3:105246830-105247167	GM12878	blood:	n/a	chr3:105247029-105247040
20	BHLHE40	chr3:105333104-105333536	K562	blood:	n/a	n/a
21	BHLHE40	chr3:105221957-105222406	HepG2	liver:	n/a	n/a
22	BHLHE40	chr3:105345658-105346016	K562	blood:	n/a	n/a
23	BHLHE40	chr3:105389966-105390094	GM12878	blood:	n/a	n/a
24	CBX3	chr3:105237573-105238047	HCT-116	colon:	n/a	n/a
25	CBX3	chr3:105333123-105333590	K562	blood:	n/a	n/a
26	CBX3	chr3:105316599-105317384	HCT-116	colon:	n/a	n/a
27	CBX3	chr3:105330157-105330875	HCT-116	colon:	n/a	n/a
28	CCNT2	chr3:105333112-105333567	K562	blood:	n/a	n/a
29	CEBPB	chr3:105240050-105240252	HepG2	liver:	n/a	chr3:105240179-105240190
30	CEBPB	chr3:105348745-105349030	A549	lung:	n/a	n/a
31	CEBPB	chr3:105345603-105346016	K562	blood:	n/a	n/a
32	CEBPB	chr3:105365938-105366287	MCF-7	breast:	n/a	chr3:105366074-105366085
33	CEBPB	chr3:105221949-105222401	HepG2	liver:	n/a	chr3:105222086-105222098 chr3:105222221-105222234
34	CEBPB	chr3:105365923-105366245	K562	blood:	n/a	chr3:105366074-105366085
35	CEBPB	chr3:105365872-105366323	HCT-116	colon:	n/a	chr3:105366074-105366085
36	CEBPB	chr3:105256241-105256887	IMR90	lung:	n/a	chr3:105256697-105256708 chr3:105256695-105256706
37	CEBPB	chr3:105218881-105219160	IMR90	lung:	n/a	chr3:105219016-105219029 chr3:105219016-105219027
38	CEBPB	chr3:105280166-105280457	HepG2	liver:	n/a	chr3:105280311-105280322
39	CEBPB	chr3:105365791-105366372	A549	lung:	n/a	chr3:105366074-105366085
40	CEBPB	chr3:105303180-105303303	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:105348849-105348920	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:105280179-105280439	A549	lung:	n/a	chr3:105280311-105280322
43	CEBPB	chr3:105303103-105303509	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:105375536-105375751	HepG2	liver:	n/a	chr3:105375617-105375628
45	CEBPB	chr3:105375508-105375758	Hela-S3	cervix:	n/a	chr3:105375617-105375628
46	CEBPB	chr3:105240060-105240260	A549	lung:	n/a	chr3:105240179-105240190
47	CEBPB	chr3:105365909-105366211	K562	blood:	n/a	chr3:105366074-105366085
48	CEBPB	chr3:105348626-105349005	IMR90	lung:	n/a	n/a
49	CEBPB	chr3:105365895-105366264	A549	lung:	n/a	chr3:105366074-105366085
50	CEBPB	chr3:105333136-105333532	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:105236259-105236309	ovcar-3	ovarian:	n/a
2	chr3:105293613-105293663	SK-N-SH	brain:	n/a
3	chr3:105333123-105333173	HMEC	breast:	n/a
4	chr3:105333123-105333173	AG04450	lung:	fetal
5	chr3:105244696-105244746	NHDF-neo	bronchial:	n/a
6	chr3:105293613-105293663	AG04450	lung:	fetal
7	chr3:105221308-105221358	HCPEpiC	choroid plexus:	n/a
8	chr3:105332022-105332072	SK-N-SH_RA	brain:	n/a
9	chr3:105332022-105332072	HEK293	kidney:	embryo
10	chr3:105247852-105247902	SKMC	muscle:	n/a
11	chr3:105228864-105228914	GM06990	blood:	n/a
12	chr3:105236259-105236309	HRCEpiC	kidney:	n/a
13	chr3:105221308-105221358	K562	blood:	n/a
14	chr3:105221308-105221358	MCF-7	breast:	n/a
15	chr3:105228864-105228914	SKMC	muscle:	n/a
16	chr3:105377640-105377690	HEEpiC	esophagus:	n/a
17	chr3:105247852-105247902	HUVEC	blood vessel:	n/a
18	chr3:105377640-105377690	Hela-S3	cervix:	n/a
19	chr3:105247852-105247902	BJ	skin:	n/a
20	chr3:105236259-105236309	SK-N-SH_RA	brain:	n/a
21	chr3:105293613-105293663	GM12878	blood:	n/a
22	chr3:105293613-105293663	NHDF-neo	bronchial:	n/a
23	chr3:105333123-105333173	NB4	blood:	n/a
24	chr3:105244696-105244746	HIPEpiC	eye:	n/a
25	chr3:105244696-105244746	LNCaP	prostate:	n/a
26	chr3:105247852-105247902	GM12878	blood:	n/a
27	chr3:105293613-105293663	U87	brain:	n/a
28	chr3:105247852-105247902	K562	blood:	n/a
29	chr3:105332022-105332072	NB4	blood:	n/a
30	chr3:105246298-105246348	NT2-D1	testis:	n/a
31	chr3:105244696-105244746	K562	blood:	n/a
32	chr3:105293613-105293663	K562	blood:	n/a
33	chr3:105333123-105333173	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:105332022-105332072	AG04449	skin:	fetal
35	chr3:105244696-105244746	HCF	heart:	n/a
36	chr3:105247852-105247902	T-47D	breast:	n/a
37	chr3:105293613-105293663	SK-N-MC	brain:	n/a
38	chr3:105221308-105221358	PrEC	prostate:	n/a
39	chr3:105247852-105247902	PrEC	prostate:	n/a
40	chr3:105299405-105299455	NH-A	brain:	n/a
41	chr3:105247852-105247902	H1-hESC	embryonic stem cell:	embryo
42	chr3:105293613-105293663	SKMC	muscle:	n/a
43	chr3:105377640-105377690	Jurkat	blood:	n/a
44	chr3:105244696-105244746	HNPCEpiC	eye:	n/a
45	chr3:105293613-105293663	H1-hESC	embryonic stem cell:	embryo
46	chr3:105228864-105228914	ovcar-3	ovarian:	n/a
47	chr3:105299405-105299455	GM06990	blood:	n/a
48	chr3:105299405-105299455	AG04450	lung:	fetal
49	chr3:105236259-105236309	GM06990	blood:	n/a
50	chr3:105293613-105293663	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:105384518..105386462-chr3:105388169..105391773,3	MCF-7	breast:
2	chr3:105215069..105217768-chr3:105217819..105220349,2	MCF-7	breast:
3	chr3:105085752..105088107-chr3:105232298..105234295,2	MCF-7	breast:
4	chr3:105215422..105217520-chr3:105229817..105232487,2	MCF-7	breast:
5	chr3:105388584..105391376-chr3:105413040..105414567,2	MCF-7	breast:
6	chr3:105326304..105329167-chr3:105329885..105331831,2	K562	blood:
7	chr3:105384518..105386462-chr3:105388169..105391773,3	MCF-7	breast:
8	chr3:105391728..105394638-chr3:105395821..105398573,2	MCF-7	breast:
9	chr3:105352013..105355360-chr3:105356310..105359089,4	K562	blood:
10	chr3:105102643..105105325-chr3:105235464..105238023,2	MCF-7	breast:
11	chr3:105084204..105086094-chr3:105239475..105242401,2	MCF-7	breast:
12	chr3:105388597..105390954-chr3:105393490..105396667,3	MCF-7	breast:
13	chr3:105235908..105237655-chr3:105242173..105244710,2	MCF-7	breast:
14	chr3:105328849..105330931-chr3:105332356..105334340,2	K562	blood:
15	chr3:105275017..105277124-chr3:105277542..105279402,2	MCF-7	breast:
16	chr3:105352621..105354226-chr3:105357589..105360065,2	K562	blood:
17	chr3:105239915..105242077-chr3:105242137..105244571,2	MCF-7	breast:
18	chr3:105239915..105242077-chr3:105242137..105244571,2	MCF-7	breast:
19	chr3:105085811..105086687-chr3:105236816..105237622,2	MCF-7	breast:
20	chr3:105259203..105260884-chr3:105262936..105265774,2	MCF-7	breast:
21	chr3:105326304..105329167-chr3:105329885..105331831,2	K562	blood:
22	chr3:105272104..105273978-chr3:105278309..105280782,2	MCF-7	breast:
23	chr3:105388597..105390954-chr3:105393490..105396667,3	MCF-7	breast:
24	chr3:105352621..105354226-chr3:105357589..105360065,2	K562	blood:
25	chr3:105235908..105237655-chr3:105242173..105244710,2	MCF-7	breast:
26	chr3:105373222..105375120-chr3:105379511..105381347,2	K562	blood:
27	chr3:105256481..105258360-chr3:105266357..105269370,3	MCF-7	breast:
28	chr3:105352013..105355360-chr3:105356310..105359089,4	K562	blood:
29	chr3:105328849..105330931-chr3:105332356..105334340,2	K562	blood:
30	chr3:105274336..105276377-chr3:105279991..105282080,2	K562	blood:
31	chr13:35938087..35938941-chr3:105372532..105373470,2	MCF-7	breast:
32	chr3:105084716..105086596-chr3:105238447..105241338,3	MCF-7	breast:
33	chr3:105087236..105090040-chr3:105234697..105237400,2	MCF-7	breast:
34	chr3:105373222..105375120-chr3:105379511..105381347,2	K562	blood:
35	chr3:105088359..105089332-chr3:105237182..105238145,2	MCF-7	breast:
36	chr3:105272104..105273978-chr3:105278309..105280782,2	MCF-7	breast:
37	chr3:105275017..105277124-chr3:105277542..105279402,2	MCF-7	breast:
38	chr3:105215069..105217768-chr3:105217819..105220349,2	MCF-7	breast:
39	chr3:105373294..105375257-chr9:136126002..136127894,2	MCF-7	breast:
40	chr3:105274336..105276377-chr3:105279991..105282080,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC54-12	chr3:105213126-105213258	ucscGeneNc_uc003dvu_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ALCAM	hsa-miR-215-5p	chr3:105293508-105293529
2	ALCAM	hsa-miR-192-5p	chr3:105291010-105291016
3	ALCAM	hsa-miR-192-5p	chr3:105293508-105293529
4	ALCAM	hsa-miR-215-5p	chr3:105291010-105291016

Variant related genes	Relation type
ALCAM	TF binding region
CBLB	TF binding region
ALCAM	CpG island
CBLB	CpG island
ENSG00000114423	chromatin interactions
ENSG00000170017	chromatin interactions

Extended variants
information (count: 6877 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6877 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545014604	chr3:105203425-105203426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77115190	chr3:105203426-105203427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78532285	chr3:105203503-105203504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117666393	chr3:105203520-105203521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76353843	chr3:105203534-105203535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531582896	chr3:105203556-105203557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116224842	chr3:105203560-105203561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs137983736	chr3:105203589-105203590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538604223	chr3:105203607-105203608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117015594	chr3:105203617-105203618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530846802	chr3:105203639-105203640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565699270	chr3:105203645-105203646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13071531	chr3:105203662-105203663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9857961	chr3:105203665-105203666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs34702307	chr3:105203673-105203674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9857705	chr3:105203693-105203694	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73854306	chr3:105203723-105203724	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186645288	chr3:105203806-105203807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191952606	chr3:105203820-105203821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545123900	chr3:105203845-105203846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560269129	chr3:105203868-105203869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144857335	chr3:105203879-105203880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542552825	chr3:105203892-105203893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561237628	chr3:105203902-105203903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138821882	chr3:105203946-105203947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550016343	chr3:105204106-105204107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141940189	chr3:105204126-105204127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532223908	chr3:105204153-105204154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547505746	chr3:105204209-105204210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10575049	chr3:105204220-105204221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs66844377	chr3:105204221-105204222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531785736	chr3:105204240-105204241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200277130	chr3:105204241-105204242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183587296	chr3:105204243-105204244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530953200	chr3:105204244-105204245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199939375	chr3:105204247-105204248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550942470	chr3:105204317-105204318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150859148	chr3:105204334-105204335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565849157	chr3:105204388-105204389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139300878	chr3:105204444-105204445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556314111	chr3:105204454-105204455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534113235	chr3:105204466-105204467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571539338	chr3:105204519-105204520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553210095	chr3:105204525-105204526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538735676	chr3:105204551-105204552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371426122	chr3:105204676-105204677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200518313	chr3:105204682-105204683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9288807	chr3:105204701-105204702	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs73189034	chr3:105204769-105204770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs149577773	chr3:105204815-105204816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2466 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105193000-105209000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:105193000-105215400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:105193200-105209400	Weak transcription	HSMM	muscle
4	chr3:105193200-105209400	Weak transcription	NH-A	brain
5	chr3:105193200-105213600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr3:105200000-105209400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:105200000-105209400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:105200200-105204000	Weak transcription	Brain Angular Gyrus	brain
9	chr3:105200400-105204600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:105200400-105204600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:105200600-105204000	Weak transcription	Brain Substantia Nigra	brain
12	chr3:105201200-105214600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:105202800-105209400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:105203400-105203600	Enhancers	Liver	Liver
15	chr3:105203400-105204000	Enhancers	Brain Cingulate Gyrus	brain
16	chr3:105203600-105206200	Weak transcription	Liver	Liver
17	chr3:105204000-105204200	Enhancers	Brain Angular Gyrus	brain
18	chr3:105204000-105204200	Enhancers	Brain Substantia Nigra	brain
19	chr3:105204000-105209200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr3:105204200-105204600	Weak transcription	Brain Angular Gyrus	brain
21	chr3:105204600-105205000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:105204600-105205000	Enhancers	Brain Angular Gyrus	brain
23	chr3:105204600-105205400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:105204600-105209400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:105205400-105205600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr3:105205400-105213800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:105205600-105209000	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr3:105206200-105207000	Enhancers	Liver	Liver
29	chr3:105206200-105207000	Enhancers	HepG2	liver
30	chr3:105206800-105207800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:105207000-105209400	Weak transcription	Liver	Liver
32	chr3:105207400-105209400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:105207600-105209400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:105207600-105209600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr3:105207800-105208000	Enhancers	Brain Anterior Caudate	brain
36	chr3:105207800-105209600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:105207800-105209600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:105208000-105209200	Weak transcription	Brain Anterior Caudate	brain
39	chr3:105208800-105209600	Enhancers	Fetal Heart	heart
40	chr3:105208800-105209600	Weak transcription	Lung	lung
41	chr3:105208800-105210200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:105209000-105209400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr3:105209000-105210200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr3:105209000-105210200	ZNF genes & repeats	A549	lung
45	chr3:105209000-105210400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
46	chr3:105209000-105210600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
47	chr3:105209200-105210000	ZNF genes & repeats	Brain Anterior Caudate	brain
48	chr3:105209200-105210200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
49	chr3:105209200-105210400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
50	chr3:105209200-105210600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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