Variant report

Variant	nsv1012260
Chromosome Location	chr3:115680931-115935968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1893)
CpG islands
(count:427)
Chromatin interactive
region (count:59)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:115858959-115859269	K562	blood:	n/a	n/a
2	ARID3A	chr3:115705465-115705645	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:115764084-115764607	K562	blood:	n/a	n/a
4	ARID3A	chr3:115758072-115759429	K562	blood:	n/a	n/a
5	ARID3A	chr3:115719033-115719603	K562	blood:	n/a	n/a
6	ARID3A	chr3:115701567-115701773	K562	blood:	n/a	n/a
7	ARID3A	chr3:115812320-115812531	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:115743333-115743461	K562	blood:	n/a	n/a
9	ARID3A	chr3:115705405-115705848	K562	blood:	n/a	n/a
10	ARID3A	chr3:115724290-115724645	K562	blood:	n/a	n/a
11	ARID3A	chr3:115778358-115778910	K562	blood:	n/a	n/a
12	ATF1	chr3:115694284-115694614	K562	blood:	n/a	n/a
13	ATF1	chr3:115719038-115719486	K562	blood:	n/a	n/a
14	ATF2	chr3:115715263-115715619	GM12878	blood:	n/a	n/a
15	ATF2	chr3:115776189-115776779	GM12878	blood:	n/a	n/a
16	ATF2	chr3:115719057-115719473	GM12878	blood:	n/a	n/a
17	ATF2	chr3:115756637-115757809	GM12878	blood:	n/a	n/a
18	ATF2	chr3:115739261-115739853	GM12878	blood:	n/a	n/a
19	ATF2	chr3:115756707-115757808	GM12878	blood:	n/a	n/a
20	ATF2	chr3:115719079-115719568	GM12878	blood:	n/a	n/a
21	ATF3	chr3:115719110-115719384	K562	blood:	n/a	n/a
22	ATF3	chr3:115719173-115719396	K562	blood:	n/a	n/a
23	BACH1	chr3:115738195-115738609	K562	blood:	n/a	n/a
24	BACH1	chr3:115758362-115758509	K562	blood:	n/a	n/a
25	BACH1	chr3:115719127-115719447	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:115719056-115719379	K562	blood:	n/a	n/a
27	BATF	chr3:115715295-115715523	GM12878	blood:	n/a	chr3:115715436-115715447
28	BATF	chr3:115756737-115757044	GM12878	blood:	n/a	n/a
29	BATF	chr3:115719144-115719536	GM12878	blood:	n/a	n/a
30	BATF	chr3:115858482-115858848	GM12878	blood:	n/a	chr3:115858669-115858679 chr3:115858668-115858679
31	BATF	chr3:115757370-115757649	GM12878	blood:	n/a	chr3:115757636-115757645
32	BATF	chr3:115739305-115739695	GM12878	blood:	n/a	chr3:115739386-115739394
33	BATF	chr3:115694191-115694522	GM12878	blood:	n/a	chr3:115694439-115694449 chr3:115694435-115694445
34	BATF	chr3:115757373-115757653	GM12878	blood:	n/a	chr3:115757636-115757645
35	BATF	chr3:115719151-115719473	GM12878	blood:	n/a	n/a
36	BATF	chr3:115756703-115757102	GM12878	blood:	n/a	n/a
37	BATF	chr3:115858497-115858790	GM12878	blood:	n/a	chr3:115858669-115858679 chr3:115858668-115858679
38	BCL11A	chr3:115757399-115757729	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:115756707-115757185	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:115756790-115757065	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:115757405-115757687	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:115739340-115739548	GM12878	blood:	n/a	n/a
43	BCL3	chr3:115756821-115757130	GM12878	blood:	n/a	n/a
44	BCL3	chr3:115719150-115719464	GM12878	blood:	n/a	chr3:115719273-115719282
45	BCLAF1	chr3:115719094-115719484	GM12878	blood:	n/a	chr3:115719273-115719282
46	BCLAF1	chr3:115756693-115757828	GM12878	blood:	n/a	n/a
47	BHLHE40	chr3:115778549-115778848	K562	blood:	n/a	n/a
48	BHLHE40	chr3:115725921-115726258	GM12878	blood:	n/a	n/a
49	BHLHE40	chr3:115739258-115739649	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:115758383-115759390	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:115724567-115724617	BE2_C	brain:	n/a
2	chr3:115758614-115758664	HIPEpiC	eye:	n/a
3	chr3:115758614-115758664	NH-A	brain:	n/a
4	chr3:115919469-115919519	HL-60	blood:	n/a
5	chr3:115752704-115752754	HRCEpiC	kidney:	n/a
6	chr3:115919469-115919519	HNPCEpiC	eye:	n/a
7	chr3:115758614-115758664	A549	lung:	n/a
8	chr3:115752704-115752754	BE2_C	brain:	n/a
9	chr3:115837501-115837551	HMEC	breast:	n/a
10	chr3:115919469-115919519	AG10803	skin:	n/a
11	chr3:115724567-115724617	ovcar-3	ovarian:	n/a
12	chr3:115724567-115724617	AG04449	skin:	fetal
13	chr3:115724567-115724617	SK-N-SH_RA	brain:	n/a
14	chr3:115724567-115724617	SK-N-MC	brain:	n/a
15	chr3:115758614-115758664	RPTEC	kidney:	n/a
16	chr3:115724567-115724617	SK-N-SH	brain:	n/a
17	chr3:115724567-115724617	HL-60	blood:	n/a
18	chr3:115752704-115752754	HMEC	breast:	n/a
19	chr3:115919469-115919519	NT2-D1	testis:	n/a
20	chr3:115919469-115919519	SK-N-MC	brain:	n/a
21	chr3:115758614-115758664	HRCEpiC	kidney:	n/a
22	chr3:115705401-115705451	NHDF-neo	bronchial:	n/a
23	chr3:115758614-115758664	K562	blood:	n/a
24	chr3:115758614-115758664	AG10803	skin:	n/a
25	chr3:115837501-115837551	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:115752704-115752754	T-47D	breast:	n/a
27	chr3:115758614-115758664	T-47D	breast:	n/a
28	chr3:115724567-115724617	HCT-116	colon:	n/a
29	chr3:115837501-115837551	HCM	heart:	n/a
30	chr3:115919469-115919519	HUVEC	blood vessel:	n/a
31	chr3:115919469-115919519	NHDF-neo	bronchial:	n/a
32	chr3:115752704-115752754	BJ	skin:	n/a
33	chr3:115919469-115919519	HepG2	liver:	n/a
34	chr3:115718524-115718574	SK-N-SH	brain:	n/a
35	chr3:115752704-115752754	PrEC	prostate:	n/a
36	chr3:115724567-115724617	NB4	blood:	n/a
37	chr3:115718524-115718574	HEK293	kidney:	embryo
38	chr3:115718524-115718574	HRE	kidney:	n/a
39	chr3:115718524-115718574	HIPEpiC	eye:	n/a
40	chr3:115705401-115705451	BJ	skin:	n/a
41	chr3:115718524-115718574	AG09319	gingival:	n/a
42	chr3:115705401-115705451	HRE	kidney:	n/a
43	chr3:115758614-115758664	CMK	blood:	n/a
44	chr3:115724567-115724617	HRCEpiC	kidney:	n/a
45	chr3:115837501-115837551	PFSK-1	brain:	n/a
46	chr3:115752704-115752754	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:115718524-115718574	H1-hESC	embryonic stem cell:	embryo
48	chr3:115718524-115718574	GM06990	blood:	n/a
49	chr3:115718524-115718574	HAEpiC	amniotic membrane:	n/a
50	chr3:115837501-115837551	GM12891	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:62608633..62609155-chr3:115772145..115772665,2	Hela-S3	cervix:
2	chr3:115779019..115780579-chr3:115783540..115785831,2	K562	blood:
3	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:
4	chr3:115858744..115859345-chr3:117437910..117438488,2	MCF-7	breast:
5	chr3:115734236..115736580-chr3:115739565..115741559,2	K562	blood:
6	chr11:62607697..62610629-chr3:115772145..115773665,2	K562	blood:
7	chr3:115721061..115723047-chr3:115724752..115726318,2	K562	blood:
8	chr3:115722266..115725111-chr3:115746899..115749615,2	K562	blood:
9	chr3:115704364..115706313-chr3:115711389..115713489,2	K562	blood:
10	chr3:115811955..115814777-chr3:115816047..115817763,3	K562	blood:
11	chr3:115770645..115772165-chr6:142364804..142366315,2	MCF-7	breast:
12	chr3:115721061..115723047-chr3:115724752..115726318,2	K562	blood:
13	chr3:115735303..115737446-chr3:115742126..115744176,2	K562	blood:
14	chr3:115862450..115863088-chr7:54350364..54350864,2	MCF-7	breast:
15	chr3:115682591..115685297-chr3:115697294..115699959,2	K562	blood:
16	chr3:115838925..115841642-chr3:115843217..115845978,2	MCF-7	breast:
17	chr3:115718424..115720399-chr3:115727607..115730544,2	K562	blood:
18	chr3:115779019..115780579-chr3:115783540..115785831,2	K562	blood:
19	chr3:115683058..115685167-chr3:115688212..115689809,2	K562	blood:
20	chr3:115844845..115847305-chr3:115848813..115850468,2	K562	blood:
21	chr3:115714015..115716158-chr3:115718030..115720877,2	K562	blood:
22	chr11:62608648..62609195-chr3:115772145..115772665,2	MCF-7	breast:
23	chr3:115735303..115737446-chr3:115742126..115744176,2	K562	blood:
24	chr3:115704364..115706313-chr3:115711389..115713489,2	K562	blood:
25	chr17:41399462..41401706-chr3:115772145..115773645,2	MCF-7	breast:
26	chr3:115734236..115736580-chr3:115739565..115741559,2	K562	blood:
27	chr3:115751729..115754397-chr3:115759672..115761602,2	K562	blood:
28	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:
29	chr11:62608624..62609620-chr3:115772145..115772665,2	NB4	blood:
30	chr3:115844845..115847305-chr3:115848813..115850468,2	K562	blood:
31	chr16:28081161..28081756-chr3:115784349..115785248,2	MCF-7	breast:
32	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
33	chr3:73160073..73160628-chr3:115771645..115772645,4	HCT-116	colon:
34	chr3:115811935..115813455-chr3:115816189..115817763,2	K562	blood:
35	chr3:115890950..115893420-chr3:115897517..115899878,2	K562	blood:
36	chr3:115683058..115685167-chr3:115688212..115689809,2	K562	blood:
37	chr3:115637962..115639771-chr3:115691041..115693586,2	K562	blood:
38	chr17:41463814..41467387-chr3:115770645..115773645,5	K562	blood:
39	chr3:115890950..115893420-chr3:115897517..115899878,2	K562	blood:
40	chr3:115682591..115685297-chr3:115697294..115699959,2	K562	blood:
41	chr3:115892441..115895134-chr9:128466129..128468903,2	MCF-7	breast:
42	chr3:115838925..115841642-chr3:115843217..115845978,2	MCF-7	breast:
43	chr11:62607723..62610629-chr3:115772165..115773665,2	K562	blood:
44	chr3:115858909..115859556-chr3:116235958..116236759,2	MCF-7	breast:
45	chr17:41464397..41466181-chr3:115772145..115773645,2	MCF-7	breast:
46	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
47	chr3:115722266..115725111-chr3:115746899..115749615,2	K562	blood:
48	chr3:73159068..73161464-chr3:115770665..115773645,3	MCF-7	breast:
49	chr3:115751729..115754397-chr3:115759672..115761602,2	K562	blood:
50	chr3:115675039..115678352-chr3:115682310..115684840,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAP43-12	chr3:115917729-115917998	uc_120_+
2	lnc-ZBTB20-4	chr3:115917729-115917998	uc_120_-
3	lnc-GAP43-11	chr3:115916157-115916457	uc_119_+
4	lnc-ZBTB20-3	chr3:115916157-115916457	uc_119_-

No data

Variant related genes	Relation type
LSAMP	TF binding region
LSAMP	CpG island
ENSG00000223247	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 8887 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:8887 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562610160	chr3:115680943-115680944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574479158	chr3:115680968-115680969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76766646	chr3:115680981-115680982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147417103	chr3:115680991-115680992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192241087	chr3:115681015-115681016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139675629	chr3:115681030-115681031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564688114	chr3:115681063-115681064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373670494	chr3:115681069-115681070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184575714	chr3:115681091-115681092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550246175	chr3:115681113-115681114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371045375	chr3:115681148-115681149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188422749	chr3:115681165-115681166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551758365	chr3:115681181-115681182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145186686	chr3:115681186-115681187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147647489	chr3:115681190-115681191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181241416	chr3:115681213-115681214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185683658	chr3:115681233-115681234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116387212	chr3:115681235-115681236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34245393	chr3:115681270-115681271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113554309	chr3:115681282-115681283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570614017	chr3:115681323-115681324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188927500	chr3:115681361-115681362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527598758	chr3:115681381-115681382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4277685	chr3:115681395-115681396	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541811073	chr3:115681410-115681411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148681886	chr3:115681435-115681436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571981262	chr3:115681444-115681445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537644007	chr3:115681450-115681451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182155962	chr3:115681451-115681452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564673831	chr3:115681492-115681493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531887516	chr3:115681526-115681527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543619890	chr3:115681539-115681540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561815332	chr3:115681571-115681572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151137874	chr3:115681577-115681578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113807378	chr3:115681610-115681611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570356617	chr3:115681613-115681614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566047806	chr3:115681614-115681615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112610793	chr3:115681632-115681633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533210831	chr3:115681635-115681636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538935025	chr3:115681690-115681691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552441839	chr3:115681700-115681701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs13075363	chr3:115681734-115681735	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538003447	chr3:115681774-115681775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556409720	chr3:115681793-115681794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9865369	chr3:115681854-115681855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187138990	chr3:115681867-115681868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192410846	chr3:115681918-115681919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180759344	chr3:115681961-115681962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538308752	chr3:115681966-115681967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545485891	chr3:115681980-115681981	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
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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115650400-115686600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:115678200-115685000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:115679000-115681000	Enhancers	Brain Cingulate Gyrus	brain
4	chr3:115679800-115681000	Enhancers	Adipose Nuclei	Adipose
5	chr3:115679800-115681000	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr3:115679800-115681000	Enhancers	Fetal Brain Female	brain
7	chr3:115679800-115681200	Enhancers	Brain Anterior Caudate	brain
8	chr3:115680200-115681200	Weak transcription	Fetal Kidney	kidney
9	chr3:115680200-115694600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:115680400-115681000	Enhancers	Brain Substantia Nigra	brain
11	chr3:115680400-115681200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr3:115680400-115681800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:115680600-115681200	Enhancers	Fetal Brain Male	brain
14	chr3:115680600-115681600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:115680800-115681600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:115681400-115681600	Enhancers	Fetal Kidney	kidney
17	chr3:115681600-115681800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:115685000-115688200	Weak transcription	Fetal Lung	lung
19	chr3:115686600-115687200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:115687200-115687400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:115687400-115687800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:115687800-115688000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:115688000-115695400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr3:115689800-115690200	Enhancers	HMEC	breast
25	chr3:115690000-115690800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:115690200-115693800	Weak transcription	HMEC	breast
27	chr3:115690800-115693400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:115693400-115695200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:115693600-115694800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr3:115693600-115695000	Enhancers	NH-A	brain
31	chr3:115693800-115694000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:115693800-115694400	Enhancers	K562	blood
33	chr3:115693800-115694800	Enhancers	HMEC	breast
34	chr3:115694000-115694200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:115694000-115694200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:115694000-115694600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:115694000-115694600	Active TSS	A549	lung
38	chr3:115694000-115695000	Enhancers	HSMM	muscle
39	chr3:115694000-115695000	Enhancers	Osteobl	bone
40	chr3:115694200-115694400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr3:115694200-115694400	Flanking Active TSS	HSMMtube	muscle
42	chr3:115694200-115694600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:115694200-115694800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr3:115694200-115695000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:115694200-115695600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr3:115694200-115702800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:115694400-115694600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:115694400-115694800	Active TSS	HSMMtube	muscle
49	chr3:115694400-115695800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:115694600-115694800	Flanking Active TSS	A549	lung

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