Variant report

Variant	nsv431824
Chromosome Location	chr2:181946115-182118559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:182104135-182104418	HepG2	liver:	n/a	n/a
2	ATF1	chr2:182085028-182085085	K562	blood:	n/a	n/a
3	ATF2	chr2:181992716-181993467	GM12878	blood:	n/a	n/a
4	ATF2	chr2:181971440-181972027	GM12878	blood:	n/a	n/a
5	ATF2	chr2:181992772-181993524	GM12878	blood:	n/a	n/a
6	ATF2	chr2:182042779-182043356	GM12878	blood:	n/a	n/a
7	ATF2	chr2:182100596-182101412	GM12878	blood:	n/a	n/a
8	ATF2	chr2:181988331-181989010	GM12878	blood:	n/a	n/a
9	ATF2	chr2:182106505-182106967	GM12878	blood:	n/a	n/a
10	ATF2	chr2:182100306-182101332	GM12878	blood:	n/a	n/a
11	ATF2	chr2:182029424-182029849	GM12878	blood:	n/a	n/a
12	ATF2	chr2:182048717-182049425	GM12878	blood:	n/a	n/a
13	ATF2	chr2:181988390-181988888	GM12878	blood:	n/a	n/a
14	ATF2	chr2:182039849-182040278	GM12878	blood:	n/a	n/a
15	ATF2	chr2:181971348-181972113	GM12878	blood:	n/a	n/a
16	ATF2	chr2:182029353-182030643	GM12878	blood:	n/a	n/a
17	BATF	chr2:182106582-182106951	GM12878	blood:	n/a	n/a
18	BATF	chr2:182042928-182043174	GM12878	blood:	n/a	n/a
19	BATF	chr2:181971450-181972019	GM12878	blood:	n/a	chr2:181971737-181971747 chr2:181971736-181971747
20	BATF	chr2:182106604-182106949	GM12878	blood:	n/a	n/a
21	BATF	chr2:181988398-181988791	GM12878	blood:	n/a	n/a
22	BATF	chr2:182100794-182101235	GM12878	blood:	n/a	n/a
23	BATF	chr2:181992841-181993511	GM12878	blood:	n/a	n/a
24	BATF	chr2:181988440-181988955	GM12878	blood:	n/a	chr2:181988871-181988881 chr2:181988867-181988877
25	BATF	chr2:181992802-181993325	GM12878	blood:	n/a	n/a
26	BATF	chr2:182042806-182043243	GM12878	blood:	n/a	n/a
27	BATF	chr2:181971473-181971999	GM12878	blood:	n/a	chr2:181971737-181971747 chr2:181971736-181971747
28	BATF	chr2:182100461-182101254	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:181992812-181993312	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:181988467-181988832	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:182100780-182101194	GM12878	blood:	n/a	n/a
32	BCL11A	chr2:182048935-182049234	GM12878	blood:	n/a	chr2:182049057-182049066
33	BCL11A	chr2:181992852-181993215	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:181971450-181971969	GM12878	blood:	n/a	chr2:181971739-181971748
35	BCL11A	chr2:182100673-182101260	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:181971486-181971877	GM12878	blood:	n/a	chr2:181971739-181971748
37	BCL3	chr2:181992866-181993292	GM12878	blood:	n/a	n/a
38	BCL3	chr2:182100696-182101197	GM12878	blood:	n/a	n/a
39	BCL3	chr2:182100794-182101102	GM12878	blood:	n/a	n/a
40	BCL3	chr2:181971413-181971912	GM12878	blood:	n/a	chr2:181971739-181971748
41	BCL3	chr2:181971560-181971846	GM12878	blood:	n/a	chr2:181971739-181971748
42	BCLAF1	chr2:182029358-182030667	GM12878	blood:	n/a	chr2:182030535-182030544
43	BCLAF1	chr2:182100783-182101188	GM12878	blood:	n/a	n/a
44	BCLAF1	chr2:182106493-182106979	GM12878	blood:	n/a	n/a
45	BCLAF1	chr2:181992668-181993302	GM12878	blood:	n/a	n/a
46	BCLAF1	chr2:182042841-182043300	GM12878	blood:	n/a	n/a
47	BCLAF1	chr2:182039900-182040421	GM12878	blood:	n/a	chr2:182040063-182040070
48	BCLAF1	chr2:181971421-181972063	GM12878	blood:	n/a	chr2:181971739-181971748
49	BCLAF1	chr2:182100639-182101294	GM12878	blood:	n/a	n/a
50	BCLAF1	chr2:181971466-181972033	GM12878	blood:	n/a	chr2:181971739-181971748

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:181987552-181987602	Caco-2	colon:	n/a
2	chr2:181971175-181971225	H1-hESC	embryonic stem cell:	embryo
3	chr2:181971175-181971225	GM12891	blood:	n/a
4	chr2:181987552-181987602	GM06990	blood:	n/a
5	chr2:181987552-181987602	NHDF-neo	bronchial:	n/a
6	chr2:181971175-181971225	BJ	skin:	n/a
7	chr2:181987552-181987602	ECC-1	luminal epithelium:	n/a
8	chr2:181971175-181971225	HNPCEpiC	eye:	n/a
9	chr2:181987552-181987602	BJ	skin:	n/a
10	chr2:181987552-181987602	AG04449	skin:	fetal
11	chr2:181971175-181971225	GM19239	blood:	n/a
12	chr2:181971175-181971225	BE2_C	brain:	n/a
13	chr2:181971175-181971225	NHDF-neo	bronchial:	n/a
14	chr2:181987552-181987602	SAEC	small airway:	n/a
15	chr2:181971175-181971225	HCT-116	colon:	n/a
16	chr2:181971175-181971225	ProgFib	skin:	n/a
17	chr2:181971175-181971225	NH-A	brain:	n/a
18	chr2:181987552-181987602	ProgFib	skin:	n/a
19	chr2:181987552-181987602	HEEpiC	esophagus:	n/a
20	chr2:181971175-181971225	HCF	heart:	n/a
21	chr2:181971175-181971225	SK-N-MC	brain:	n/a
22	chr2:181987552-181987602	BE2_C	brain:	n/a
23	chr2:181987552-181987602	K562	blood:	n/a
24	chr2:181987552-181987602	AG09319	gingival:	n/a
25	chr2:181987552-181987602	AG09309	skin:	n/a
26	chr2:181987552-181987602	HRE	kidney:	n/a
27	chr2:181987552-181987602	HepG2	liver:	n/a
28	chr2:181987552-181987602	SK-N-MC	brain:	n/a
29	chr2:181971175-181971225	HRPEpiC	eye:	n/a
30	chr2:181971175-181971225	AG04450	lung:	fetal
31	chr2:181987552-181987602	RPTEC	kidney:	n/a
32	chr2:181987552-181987602	AG10803	skin:	n/a
33	chr2:181987552-181987602	HCT-116	colon:	n/a
34	chr2:181971175-181971225	NB4	blood:	n/a
35	chr2:181971175-181971225	U87	brain:	n/a
36	chr2:181987552-181987602	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:181987552-181987602	LNCaP	prostate:	n/a
38	chr2:181987552-181987602	A549	lung:	n/a
39	chr2:181987552-181987602	GM19239	blood:	n/a
40	chr2:181971175-181971225	Caco-2	colon:	n/a
41	chr2:181987552-181987602	SK-N-SH	brain:	n/a
42	chr2:181971175-181971225	HCPEpiC	choroid plexus:	n/a
43	chr2:181987552-181987602	NH-A	brain:	n/a
44	chr2:181987552-181987602	PANC-1	pancreas:	n/a
45	chr2:181987552-181987602	HIPEpiC	eye:	n/a
46	chr2:181971175-181971225	PFSK-1	brain:	n/a
47	chr2:181971175-181971225	MCF-7	breast:	n/a
48	chr2:181987552-181987602	HNPCEpiC	eye:	n/a
49	chr2:181987552-181987602	GM12878	blood:	n/a
50	chr2:181971175-181971225	HAEpiC	amniotic membrane:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:182103920..182104651-chr2:182331149..182331746,3	MCF-7	breast:
2	chr2:182096231..182098088-chr2:182100894..182102603,2	K562	blood:
3	chr2:182073844..182076497-chr2:182076858..182079352,2	K562	blood:
4	chr2:182073844..182076497-chr2:182076858..182079352,2	K562	blood:
5	chr2:182013926..182016725-chr2:182035700..182038475,2	K562	blood:
6	chr2:182100728..182102852-chr2:182270118..182272458,2	MCF-7	breast:
7	chr12:45761490..45762324-chr2:181950979..181951563,2	MCF-7	breast:
8	chr2:182013926..182016725-chr2:182035700..182038475,2	K562	blood:
9	chr2:182095672..182098077-chr2:182098545..182101336,2	K562	blood:
10	chr2:182067091..182069385-chr2:182080584..182082731,2	K562	blood:
11	chr2:181839506..181842433-chr2:181971642..181974430,2	K562	blood:
12	chr2:181969275..181969953-chr2:182330780..182331934,4	MCF-7	breast:
13	chr2:182095672..182098077-chr2:182098545..182101336,2	K562	blood:
14	chr2:181941490..181943748-chr2:181947073..181949611,2	K562	blood:
15	chr2:181984288..181986201-chr2:181987328..181989334,2	MCF-7	breast:
16	chr2:182096231..182098088-chr2:182100894..182102603,2	K562	blood:
17	chr2:181849955..181852390-chr2:181948702..181951416,2	K562	blood:
18	chr2:181969337..181969909-chr2:182579643..182580293,2	MCF-7	breast:
19	chr2:181968911..181970241-chr2:182330712..182332033,4	MCF-7	breast:
20	chr2:182067091..182069385-chr2:182080584..182082731,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CERKL-2	chr2:181993130-181993574	NONHSAT075862
2	lnc-UBE2E3-1	chr2:181973624-181973656	XLOC_001776
3	lnc-CERKL-2	chr2:181970580-181970695	XLOC_002417
4	lnc-UBE2E3-1	chr2:181988623-181988707	XLOC_001776
5	lnc-CERKL-2	chr2:181991894-181992422	NONHSAT075862
6	lnc-UBE2E3-1	chr2:181988564-181988707	ENSG00000234663
7	lnc-UBE2E3-1	chr2:181988669-181988707	XLOC_001776
8	lnc-CERKL-2	chr2:181962209-181962315	XLOC_002417
9	lnc-UBE2E3-1	chr2:182091198-182091262	XLOC_001776
10	lnc-UBE2E3-4	chr2:181971351-181972525	ucscGeneNc_uc002uns_1
11	lnc-UBE2E3-1	chr2:181966659-181966759	XLOC_001776
12	lnc-UBE2E3-1	chr2:181988659-181988707	XLOC_001776
13	lnc-UBE2E3-1	chr2:182056649-182056780	XLOC_001776
14	lnc-CERKL-2	chr2:181968728-181968784	XLOC_002417
15	lnc-CERKL-2	chr2:181968206-181968283	XLOC_002417
16	lnc-UBE2E3-1	chr2:181988562-181988707	XLOC_001776
17	lnc-UBE2E3-1	chr2:182102978-182103177	XLOC_001776
18	lnc-UBE2E3-1	chr2:181976709-181976784	XLOC_001776
19	lnc-UBE2E3-1	chr2:182091198-182091262	ENSG00000234663
20	lnc-CERKL-2	chr2:181970580-181970695	NONHSAT075862
21	lnc-CERKL-2	chr2:182028673-182029275	NONHSAT075862
22	lnc-UBE2E3-1	chr2:181988564-181988707	XLOC_001776
23	lnc-UBE2E3-1	chr2:182091198-182091262	XLOC_001776
24	lnc-CERKL-2	chr2:181988623-181988706	NONHSAT075862
25	lnc-UBE2E3-1	chr2:182091198-182091262	XLOC_001776
26	lnc-CERKL-5	chr2:182029520-182030027	predAs_ge08_ITGA4_1
27	lnc-UBE2E3-1	chr2:182091198-182091262	XLOC_001776

No data

Variant related genes	Relation type
ENSG00000234663	TF binding region
ENSG00000238171	TF binding region
ENSG00000234663	CpG island
ENSG00000238171	CpG island
ENSG00000234663	chromatin interactions
MORF4L2	miRNA target sites
NSFL1C	miRNA target sites
ATAD2	miRNA target sites
E2F1	miRNA target sites
TBPL1	miRNA target sites
TBRG1	miRNA target sites
TGFBR1	miRNA target sites
NAP1L2	miRNA target sites
TSPAN6	miRNA target sites
JAK1	miRNA target sites

Extended variants
information (count: 5612 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:5612 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10184839	chr2:181946115-181946116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10184846	chr2:181946132-181946133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs543999887	chr2:181946157-181946158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146070219	chr2:181946171-181946172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187302194	chr2:181946173-181946174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540525464	chr2:181946178-181946179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191837655	chr2:181946201-181946202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10208742	chr2:181946208-181946209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs78657765	chr2:181946305-181946306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545386599	chr2:181946309-181946310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565157175	chr2:181946316-181946317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530987621	chr2:181946354-181946355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184850159	chr2:181946398-181946399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567836397	chr2:181946409-181946410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189363212	chr2:181946652-181946653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372073611	chr2:181946689-181946690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180917552	chr2:181946792-181946793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535155212	chr2:181946796-181946797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116783351	chr2:181946822-181946823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558500753	chr2:181946880-181946881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568765655	chr2:181946913-181946914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537906970	chr2:181946972-181946973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554408531	chr2:181946996-181946997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200239150	chr2:181947052-181947053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146992206	chr2:181947053-181947054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201360824	chr2:181947057-181947058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111731575	chr2:181947058-181947059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200501011	chr2:181947060-181947061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574683173	chr2:181947086-181947087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57701847	chr2:181947089-181947090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200824547	chr2:181947096-181947097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138969042	chr2:181947132-181947133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567311677	chr2:181947148-181947149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386653265	chr2:181947162-181947163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11883509	chr2:181947163-181947164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs377297374	chr2:181947186-181947187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565242614	chr2:181947253-181947254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184144314	chr2:181947340-181947341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544687183	chr2:181947346-181947347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78273750	chr2:181947354-181947355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1356549	chr2:181947395-181947396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs79083500	chr2:181947400-181947401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546757909	chr2:181947438-181947439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10497575	chr2:181947480-181947481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs142994045	chr2:181947513-181947514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554139936	chr2:181947529-181947530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147042832	chr2:181947531-181947532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568826272	chr2:181947546-181947547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs36112667	chr2:181947554-181947555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13019038	chr2:181947634-181947635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

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
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181920800-181949800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:181934800-181947800	Weak transcription	Ovary	ovary
3	chr2:181935000-181948000	Weak transcription	Small Intestine	intestine
4	chr2:181935600-181946200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr2:181937800-181949600	Weak transcription	HSMMtube	muscle
6	chr2:181938400-181954800	Weak transcription	Psoas Muscle	Psoas
7	chr2:181939400-181948200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:181939400-181953000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:181940400-181946200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:181941200-181948800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:181942800-181950200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:181943600-181946200	Enhancers	Fetal Heart	heart
13	chr2:181945600-181946600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:181946000-181946600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:181946000-181946600	Enhancers	HUVEC	blood vessel
16	chr2:181946200-181946400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:181946200-181946400	Enhancers	Primary hematopoietic stem cells	blood
18	chr2:181946600-181949200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:181947200-181947800	Weak transcription	Aorta	Aorta
20	chr2:181947800-181948000	ZNF genes & repeats	Aorta	Aorta
21	chr2:181947800-181948000	Enhancers	Ovary	ovary
22	chr2:181948000-181949200	Weak transcription	Aorta	Aorta
23	chr2:181948800-181950000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:181948800-181950000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:181960400-181961000	Enhancers	Adipose Nuclei	Adipose
26	chr2:181961600-181962000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:181964000-181964800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:181967600-181967800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:181967800-181970800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:181968000-181968200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:181968400-181969600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr2:181969000-181969200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:181969000-181972400	Enhancers	Dnd41	blood
34	chr2:181969000-181974600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:181969200-181969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:181969200-181969800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:181969200-181970400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:181969200-181970800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr2:181969200-181972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:181969200-181972400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:181969200-181972600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr2:181969200-181973200	Enhancers	Primary T cells from cord blood	blood
43	chr2:181969200-181973200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr2:181969200-181973600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr2:181969200-181974200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr2:181969400-181969600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:181969400-181969600	Enhancers	A549	lung
48	chr2:181969400-181969600	Flanking Active TSS	GM12878-XiMat	blood
49	chr2:181969400-181969800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:181969400-181970000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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