Variant report

Variant	nsv518790
Chromosome Location	chr2:178963445-179000291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1285)
CpG islands
(count:1528)
Chromatin interactive
region (count:59)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178997076-178997318	K562	blood:	n/a	n/a
2	ARID3A	chr2:178976898-178977429	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:178997055-178997328	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:178976920-178977251	K562	blood:	n/a	n/a
5	ARID3A	chr2:178974581-178974935	K562	blood:	n/a	n/a
6	ARID3A	chr2:178974597-178974930	HepG2	liver:	n/a	n/a
7	ATF2	chr2:178976877-178977311	GM12878	blood:	n/a	n/a
8	ATF2	chr2:178976920-178977397	GM12878	blood:	n/a	n/a
9	ATF2	chr2:178976825-178977263	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:178976818-178977303	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr2:178976882-178977268	K562	blood:	n/a	n/a
12	ATF3	chr2:178976839-178977460	A549	lung:	n/a	n/a
13	BACH1	chr2:178976842-178977310	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:178976994-178977120	K562	blood:	n/a	n/a
15	BCL3	chr2:178976708-178977347	A549	lung:	n/a	chr2:178977137-178977145
16	BCL3	chr2:178976764-178977570	A549	lung:	n/a	chr2:178977137-178977145
17	BCLAF1	chr2:178976838-178977436	GM12878	blood:	n/a	chr2:178977137-178977145
18	BCLAF1	chr2:178976884-178977609	GM12878	blood:	n/a	chr2:178977137-178977145
19	BCLAF1	chr2:178976940-178977327	K562	blood:	n/a	chr2:178977137-178977145
20	BHLHE40	chr2:178976965-178977652	GM12878	blood:	n/a	chr2:178977085-178977101
21	BHLHE40	chr2:178976931-178977398	K562	blood:	n/a	chr2:178977085-178977101
22	BRCA1	chr2:178976977-178977271	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:178976944-178977264	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr2:178976932-178977574	HepG2	liver:	n/a	n/a
25	BRCA1	chr2:178976874-178977278	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr2:178976748-178977833	HCT-116	colon:	n/a	n/a
27	CBX3	chr2:178976858-178977273	K562	blood:	n/a	n/a
28	CBX3	chr2:178966009-178966407	K562	blood:	n/a	n/a
29	CBX3	chr2:178976819-178977515	K562	blood:	n/a	n/a
30	CBX3	chr2:178976684-178977547	HCT-116	colon:	n/a	n/a
31	CCNT2	chr2:178976937-178977633	K562	blood:	n/a	n/a
32	CEBPB	chr2:178976675-178977379	K562	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
33	CEBPB	chr2:178976565-178977402	MCF-7	breast:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
34	CEBPB	chr2:178976753-178977242	ECC-1	luminal epithelium:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
35	CEBPB	chr2:178976727-178977298	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
36	CEBPB	chr2:178976600-178977396	A549	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
37	CEBPB	chr2:178976623-178977534	HCT-116	colon:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
38	CEBPB	chr2:178976727-178977277	A549	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
39	CEBPB	chr2:178976832-178977171	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
40	CEBPB	chr2:178976811-178977235	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
41	CEBPB	chr2:178974078-178974316	IMR90	lung:	n/a	chr2:178974181-178974192
42	CEBPB	chr2:178976807-178977202	A549	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
43	CEBPB	chr2:178976675-178977347	MCF-7	breast:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
44	CEBPB	chr2:178974022-178974343	HepG2	liver:	n/a	chr2:178974181-178974192
45	CEBPB	chr2:178976775-178977353	Hela-S3	cervix:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
46	CEBPB	chr2:178976441-178977526	HCT-116	colon:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
47	CEBPB	chr2:178978943-178978969	A549	lung:	n/a	n/a
48	CEBPB	chr2:178976811-178977243	K562	blood:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
49	CEBPB	chr2:178976809-178977343	HepG2	liver:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013
50	CEBPB	chr2:178976793-178977216	IMR90	lung:	n/a	chr2:178977004-178977013 chr2:178977002-178977015 chr2:178977002-178977013

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178970574-178970624	HCF	heart:	n/a
2	chr2:178977079-178977129	K562	blood:	n/a
3	chr2:178977341-178977391	HEEpiC	esophagus:	n/a
4	chr2:178970574-178970624	HCF	heart:	n/a
5	chr2:178977079-178977129	K562	blood:	n/a
6	chr2:178977341-178977391	HEEpiC	esophagus:	n/a
7	chr2:178973092-178973142	AG10803	skin:	n/a
8	chr2:178976361-178976411	MCF10A-Er-Src	breast:	n/a
9	chr2:178993596-178993646	AG04449	skin:	fetal
10	chr2:178977094-178977144	NB4	blood:	n/a
11	chr2:178973251-178973301	A549	lung:	n/a
12	chr2:178973019-178973069	NH-A	brain:	n/a
13	chr2:178977079-178977129	HepG2	liver:	n/a
14	chr2:178977002-178977052	PFSK-1	brain:	n/a
15	chr2:178973147-178973197	GM12891	blood:	n/a
16	chr2:178977079-178977129	NB4	blood:	n/a
17	chr2:178977094-178977144	Caco-2	colon:	n/a
18	chr2:178977979-178978029	MCF-7	breast:	n/a
19	chr2:178973079-178973129	HRPEpiC	eye:	n/a
20	chr2:178993596-178993646	BE2_C	brain:	n/a
21	chr2:178977341-178977391	ECC-1	luminal epithelium:	n/a
22	chr2:178993596-178993646	HRCEpiC	kidney:	n/a
23	chr2:178993596-178993646	NH-A	brain:	n/a
24	chr2:178973092-178973142	HCM	heart:	n/a
25	chr2:178975712-178975762	HCT-116	colon:	n/a
26	chr2:178975712-178975762	NT2-D1	testis:	n/a
27	chr2:178973164-178973214	AoSMC	blood vessel:	n/a
28	chr2:178974175-178974225	PANC-1	pancreas:	n/a
29	chr2:178977341-178977391	AG10803	skin:	n/a
30	chr2:178975712-178975762	AoSMC	blood vessel:	n/a
31	chr2:178973019-178973069	HRE	kidney:	n/a
32	chr2:178977215-178977265	NB4	blood:	n/a
33	chr2:178973251-178973301	ovcar-3	ovarian:	n/a
34	chr2:178977818-178977868	IMR90	lung:	fetal
35	chr2:178977818-178977868	HCPEpiC	choroid plexus:	n/a
36	chr2:178973216-178973266	AG09309	skin:	n/a
37	chr2:178976981-178977031	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:178970574-178970624	MCF-7	breast:	n/a
39	chr2:178973147-178973197	HCT-116	colon:	n/a
40	chr2:178976295-178976345	PANC-1	pancreas:	n/a
41	chr2:178973147-178973197	HIPEpiC	eye:	n/a
42	chr2:178993596-178993646	MCF-7	breast:	n/a
43	chr2:178970574-178970624	AoSMC	blood vessel:	n/a
44	chr2:178973092-178973142	NB4	blood:	n/a
45	chr2:178977341-178977391	GM19239	blood:	n/a
46	chr2:178973065-178973115	SAEC	small airway:	n/a
47	chr2:178977094-178977144	HCF	heart:	n/a
48	chr2:178973164-178973214	HepG2	liver:	n/a
49	chr2:178976981-178977031	HCM	heart:	n/a
50	chr2:178976361-178976411	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:178976973..178979935-chr2:178988410..178990810,2	K562	blood:
2	chr2:178970656..178974678-chr2:178975520..178979270,3	K562	blood:
3	chr2:178978462..178980467-chr2:179057158..179058664,2	MCF-7	breast:
4	chr2:178982755..178985967-chr2:178987271..178990939,3	K562	blood:
5	chr2:178972756..178975132-chr2:178975866..178978416,2	MCF-7	breast:
6	chr2:178970656..178974678-chr2:178975520..178979270,3	K562	blood:
7	chr2:178960724..178963095-chr2:178966189..178968403,2	MCF-7	breast:
8	chr2:178981148..178983862-chr2:179057589..179059906,2	MCF-7	breast:
9	chr2:178965236..178967731-chr2:178970870..178972647,2	K562	blood:
10	chr2:178974271..178975212-chr2:179283614..179284146,3	MCF-7	breast:
11	chr2:178975067..178978289-chr2:179058254..179060575,4	MCF-7	breast:
12	chr2:178998158..179000091-chr2:179001062..179003808,2	K562	blood:
13	chr2:178987630..178989492-chr2:178991140..178993708,2	K562	blood:
14	chr2:178974532..178975128-chr2:179279107..179279741,2	MCF-7	breast:
15	chr2:178976808..178978488-chr2:179342162..179344754,2	MCF-7	breast:
16	chr2:178976079..178979038-chr2:178986555..178992721,6	MCF-7	breast:
17	chr2:178991876..178994492-chr2:179011398..179013023,2	K562	blood:
18	chr2:178974519..178975080-chr2:179279294..179279980,2	MCF-7	breast:
19	chr2:178981363..178983943-chr2:179315477..179318383,2	K562	blood:
20	chr2:178997047..178997691-chr2:179278995..179280004,3	K562	blood:
21	chr2:178976079..178979038-chr2:178986555..178992721,6	MCF-7	breast:
22	chr2:178972756..178975132-chr2:178975866..178978416,2	MCF-7	breast:
23	chr2:178982755..178985967-chr2:178987271..178990939,3	K562	blood:
24	chr2:178985318..178987568-chr2:178999084..179001889,3	K562	blood:
25	chr2:178977795..178981676-chr2:178993113..178997821,5	K562	blood:
26	chr2:178973629..178974622-chr2:179240854..179241453,2	MCF-7	breast:
27	chr2:178996470..178998861-chr2:179058707..179060776,2	MCF-7	breast:
28	chr2:178978517..178980297-chr2:179707105..179709962,2	K562	blood:
29	chr2:178991568..178995332-chr2:178996165..178998325,3	MCF-7	breast:
30	chr2:178996756..178997699-chr2:179073384..179074155,3	MCF-7	breast:
31	chr2:178955531..178957949-chr2:178963225..178965293,2	K562	blood:
32	chr2:178980858..178983485-chr2:178983971..178985850,2	K562	blood:
33	chr2:178991529..178993061-chr2:178994695..178997315,2	K562	blood:
34	chr2:178996751..178997649-chr2:179144316..179145071,2	MCF-7	breast:
35	chr2:178977125..178980608-chr2:178981010..178983814,6	K562	blood:
36	chr2:178975761..178978600-chr2:179056476..179059620,3	K562	blood:
37	chr2:178977351..178979746-chr2:178983845..178986068,3	K562	blood:
38	chr2:178997683..178998228-chr2:179261829..179262407,2	K562	blood:
39	chr2:178985399..178987987-chr2:179314612..179317404,2	MCF-7	breast:
40	chr2:178991529..178993061-chr2:178994695..178997315,2	K562	blood:
41	chr2:178977222..178979193-chr2:179277270..179279929,2	MCF-7	breast:
42	chr2:178977795..178981676-chr2:178993113..178997821,5	K562	blood:
43	chr2:178986165..178987742-chr2:178994216..178996447,2	K562	blood:
44	chr2:178975231..178977429-chr2:179315218..179317152,2	MCF-7	breast:
45	chr2:178979115..178980922-chr2:179059390..179062250,2	K562	blood:
46	chr2:178993079..178995697-chr2:179002423..179004658,2	K562	blood:
47	chr2:178974721..178975261-chr2:179285955..179286795,2	K562	blood:
48	chr2:178976973..178979935-chr2:178988410..178990810,2	K562	blood:
49	chr2:178974133..178981122-chr2:179276785..179281060,9	K562	blood:
50	chr2:178847948..178848513-chr2:178974436..178975057,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSBPL6-3	chr2:178998588-178998627	NONHSAT075737
2	lnc-OSBPL6-3	chr2:178990866-178990911	NONHSAT075737
3	lnc-RBM45-1	chr2:178999339-178999653	ucscGeneNc_uc002umb_1
4	lnc-RBM45-1	chr2:178986636-178987086	ucscGeneNc_uc002umb_1

No data

Variant related genes	Relation type
CYCTP	TF binding region
PDE11A	TF binding region
RBM45	TF binding region
ENSG00000227241	TF binding region
CYCTP	CpG island
PDE11A	CpG island
RBM45	CpG island
ENSG00000227241	CpG island
ENSG00000180228	chromatin interactions
ENSG00000155636	chromatin interactions
ENSG00000079150	chromatin interactions
ENSG00000223960	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000128655	chromatin interactions
ENSG00000079156	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551909635	chr2:178965393-178965394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs566966148	chr2:178965546-178965547	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs189988832	chr2:178965643-178965644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs147892369	chr2:178965674-178965675	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs62176007	chr2:178965869-178965870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35229453	chr2:178965909-178965910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576861208	chr2:178965918-178965919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546006024	chr2:178965920-178965921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549879165	chr2:178965984-178965985	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562526408	chr2:178965986-178965987	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs576150050	chr2:178965991-178965992	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541740692	chr2:178966007-178966008	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145348163	chr2:178966035-178966036	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs372625645	chr2:178966040-178966041	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181113884	chr2:178966114-178966115	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186517385	chr2:178966183-178966184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs533248218	chr2:178966227-178966228	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550386147	chr2:178966324-178966325	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs34395717	chr2:178966341-178966342	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78476823	chr2:178966370-178966371	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs549707316	chr2:178966379-178966380	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs151019127	chr2:178966381-178966382	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375472306	chr2:178966437-178966438	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs71423553	chr2:178966459-178966460	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553465821	chr2:178966468-178966469	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs189455474	chr2:178966586-178966587	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs547948423	chr2:178966593-178966594	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs534141950	chr2:178966608-178966609	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs140892159	chr2:178966616-178966617	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554197424	chr2:178966715-178966716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556193678	chr2:178966737-178966738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575833418	chr2:178966738-178966739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373152390	chr2:178966742-178966743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565802990	chr2:178966849-178966850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201019394	chr2:178966858-178966859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570213598	chr2:178966870-178966871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150159884	chr2:178966881-178966882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561690382	chr2:178966889-178966890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542732598	chr2:178966903-178966904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180990328	chr2:178966957-178966958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541057079	chr2:178966998-178966999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145567343	chr2:178967004-178967005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533325634	chr2:178967005-178967006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570430244	chr2:178967042-178967043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563755311	chr2:178967068-178967069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536601155	chr2:178967076-178967077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529551748	chr2:178967092-178967093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539352788	chr2:178967100-178967101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576128581	chr2:178967106-178967107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140320758	chr2:178967117-178967118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	21720365	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178965800-178966400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:178966000-178966600	Enhancers	K562	blood
3	chr2:178966000-178966600	Enhancers	NHDF-Ad	bronchial
4	chr2:178966600-178970400	Weak transcription	K562	blood
5	chr2:178967800-178968800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:178970400-178970600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:178970400-178970600	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr2:178970400-178971200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:178971200-178976800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:178973000-178973200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:178973200-178977000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:178974800-178975000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr2:178975000-178976400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr2:178975600-178976600	Enhancers	NHEK	skin
15	chr2:178976200-178976400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr2:178976400-178976600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:178976400-178976600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:178976400-178976600	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr2:178976400-178976600	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr2:178976400-178976600	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr2:178976400-178976600	Enhancers	Dnd41	blood
22	chr2:178976400-178976800	Enhancers	Primary T cells from cord blood	blood
23	chr2:178976400-178976800	Enhancers	Primary T cells fromperipheralblood	blood
24	chr2:178976400-178976800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr2:178976400-178976800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr2:178976400-178976800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr2:178976400-178976800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr2:178976400-178976800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:178976400-178976800	Enhancers	Placenta	Placenta
30	chr2:178976400-178976800	Enhancers	Hela-S3	cervix
31	chr2:178976400-178976800	Enhancers	HMEC	breast
32	chr2:178976400-178977000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr2:178976600-178976800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:178976600-178976800	Enhancers	Primary B cells from peripheral blood	blood
35	chr2:178976600-178976800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr2:178976600-178976800	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr2:178976600-178976800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:178976600-178976800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:178976600-178976800	Enhancers	Adipose Nuclei	Adipose
40	chr2:178976600-178976800	Enhancers	Brain Anterior Caudate	brain
41	chr2:178976600-178976800	Enhancers	Brain Substantia Nigra	brain
42	chr2:178976600-178976800	Enhancers	Stomach Smooth Muscle	stomach
43	chr2:178976600-178976800	Enhancers	HepG2	liver
44	chr2:178976600-178977000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:178976600-178977000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:178976600-178977000	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr2:178976600-178977000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr2:178976600-178977000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr2:178976600-178977000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:178976600-178977000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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