Variant report

Variant	nsv583910
Chromosome Location	chr2:181975252-182040293
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:182039849-182040278	GM12878	blood:	n/a	n/a
2	ATF2	chr2:181992772-181993524	GM12878	blood:	n/a	n/a
3	ATF2	chr2:182029424-182029849	GM12878	blood:	n/a	n/a
4	ATF2	chr2:182029353-182030643	GM12878	blood:	n/a	n/a
5	ATF2	chr2:181988331-181989010	GM12878	blood:	n/a	n/a
6	ATF2	chr2:181992716-181993467	GM12878	blood:	n/a	n/a
7	ATF2	chr2:181988390-181988888	GM12878	blood:	n/a	n/a
8	BATF	chr2:181988398-181988791	GM12878	blood:	n/a	n/a
9	BATF	chr2:181988440-181988955	GM12878	blood:	n/a	chr2:181988871-181988881 chr2:181988867-181988877
10	BATF	chr2:181992841-181993511	GM12878	blood:	n/a	n/a
11	BATF	chr2:181992802-181993325	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:181992852-181993215	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:181988467-181988832	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:181992812-181993312	GM12878	blood:	n/a	n/a
15	BCL3	chr2:181992866-181993292	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:181992797-181993474	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:182039900-182040421	GM12878	blood:	n/a	chr2:182040063-182040070
18	BCLAF1	chr2:181988271-181988945	GM12878	blood:	n/a	chr2:181988869-181988878
19	BCLAF1	chr2:181992668-181993302	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:182029358-182030667	GM12878	blood:	n/a	chr2:182030535-182030544
21	BHLHE40	chr2:182035018-182035182	GM12878	blood:	n/a	chr2:182035065-182035078 chr2:182035061-182035082
22	BHLHE40	chr2:181988446-181988761	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:181992839-181993263	GM12878	blood:	n/a	n/a
24	CEBPB	chr2:182023264-182023526	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:182003562-182003853	A549	lung:	n/a	chr2:182003704-182003721
26	CEBPB	chr2:182005176-182005452	MCF-7	breast:	n/a	chr2:182005350-182005361 chr2:182005348-182005365
27	CEBPB	chr2:182005234-182005411	HepG2	liver:	n/a	chr2:182005350-182005361 chr2:182005348-182005365
28	CEBPB	chr2:181992769-181993461	GM12878	blood:	n/a	n/a
29	CEBPB	chr2:182003556-182003867	IMR90	lung:	n/a	chr2:182003704-182003721
30	CEBPB	chr2:182005210-182005484	A549	lung:	n/a	chr2:182005350-182005361 chr2:182005348-182005365
31	CEBPB	chr2:182005201-182005522	Hela-S3	cervix:	n/a	chr2:182005350-182005361 chr2:182005348-182005365
32	CEBPB	chr2:181988319-181989251	GM12878	blood:	n/a	n/a
33	CEBPB	chr2:182029388-182030499	GM12878	blood:	n/a	n/a
34	CEBPB	chr2:182005155-182005548	A549	lung:	n/a	chr2:182005350-182005361 chr2:182005348-182005365
35	CEBPB	chr2:182036196-182036409	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:182003572-182003872	Hela-S3	cervix:	n/a	chr2:182003704-182003721
37	CHD2	chr2:181992933-181993287	GM12878	blood:	n/a	n/a
38	CHD2	chr2:181982084-181982093	HepG2	liver:	n/a	n/a
39	CHD2	chr2:181988491-181988834	GM12878	blood:	n/a	n/a
40	CTCF	chr2:182037572-182037674	Lung_OC	lung:	n/a	n/a
41	CTCF	chr2:182009680-182009830	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr2:182023700-182023850	HepG2	liver:	n/a	n/a
43	CTCF	chr2:182026852-182026925	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr2:182012900-182013050	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr2:182026844-182026920	LNCaP	prostate:	n/a	n/a
46	CTCF	chr2:182007213-182007307	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr2:182023760-182023910	GM12875	blood:	n/a	n/a
48	CTCF	chr2:182009713-182009734	HepG2	liver:	n/a	n/a
49	CTCF	chr2:182023753-182023907	HepG2	liver:	n/a	n/a
50	CTCF	chr2:181981939-181982029	Lung_OC	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:181987552-181987602	HRE	kidney:	n/a
2	chr2:181987552-181987602	AoSMC	blood vessel:	n/a
3	chr2:181987552-181987602	K562	blood:	n/a
4	chr2:181987552-181987602	NHBE	bronchial:	n/a
5	chr2:181987552-181987602	MCF10A-Er-Src	breast:	n/a
6	chr2:181987552-181987602	CMK	blood:	n/a
7	chr2:181987552-181987602	PANC-1	pancreas:	n/a
8	chr2:181987552-181987602	T-47D	breast:	n/a
9	chr2:181987552-181987602	GM19239	blood:	n/a
10	chr2:181987552-181987602	PrEC	prostate:	n/a
11	chr2:181987552-181987602	AG04450	lung:	fetal
12	chr2:181987552-181987602	NHDF-neo	bronchial:	n/a
13	chr2:181987552-181987602	HRPEpiC	eye:	n/a
14	chr2:181987552-181987602	HRCEpiC	kidney:	n/a
15	chr2:181987552-181987602	SAEC	small airway:	n/a
16	chr2:181987552-181987602	NH-A	brain:	n/a
17	chr2:181987552-181987602	HAEpiC	amniotic membrane:	n/a
18	chr2:181987552-181987602	SK-N-MC	brain:	n/a
19	chr2:181987552-181987602	HNPCEpiC	eye:	n/a
20	chr2:181987552-181987602	HCM	heart:	n/a
21	chr2:181987552-181987602	HEK293	kidney:	embryo
22	chr2:181987552-181987602	NB4	blood:	n/a
23	chr2:181987552-181987602	GM12892	blood:	n/a
24	chr2:181987552-181987602	SK-N-SH_RA	brain:	n/a
25	chr2:181987552-181987602	RPTEC	kidney:	n/a
26	chr2:181987552-181987602	GM12891	blood:	n/a
27	chr2:181987552-181987602	Hepatocyte	liver:	n/a
28	chr2:181987552-181987602	A549	lung:	n/a
29	chr2:181987552-181987602	Jurkat	blood:	n/a
30	chr2:181987552-181987602	NT2-D1	testis:	n/a
31	chr2:181987552-181987602	HIPEpiC	eye:	n/a
32	chr2:181987552-181987602	BE2_C	brain:	n/a
33	chr2:181987552-181987602	AG10803	skin:	n/a
34	chr2:181987552-181987602	HMEC	breast:	n/a
35	chr2:181987552-181987602	H1-hESC	embryonic stem cell:	embryo
36	chr2:181987552-181987602	PFSK-1	brain:	n/a
37	chr2:181987552-181987602	ECC-1	luminal epithelium:	n/a
38	chr2:181987552-181987602	AG09309	skin:	n/a
39	chr2:181987552-181987602	HCPEpiC	choroid plexus:	n/a
40	chr2:181987552-181987602	HCF	heart:	n/a
41	chr2:181987552-181987602	SK-N-SH	brain:	n/a
42	chr2:181987552-181987602	Hela-S3	cervix:	n/a
43	chr2:181987552-181987602	GM12878	blood:	n/a
44	chr2:181987552-181987602	BJ	skin:	n/a
45	chr2:181987552-181987602	GM06990	blood:	n/a
46	chr2:181987552-181987602	Caco-2	colon:	n/a
47	chr2:181987552-181987602	ProgFib	skin:	n/a
48	chr2:181987552-181987602	LNCaP	prostate:	n/a
49	chr2:181987552-181987602	HepG2	liver:	n/a
50	chr2:181987552-181987602	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:182013926..182016725-chr2:182035700..182038475,2	K562	blood:
2	chr2:182013926..182016725-chr2:182035700..182038475,2	K562	blood:
3	chr2:181984288..181986201-chr2:181987328..181989334,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CERKL-2	chr2:181993130-181993574	NONHSAT075862
2	lnc-UBE2E3-1	chr2:181988669-181988707	XLOC_001776
3	lnc-UBE2E3-1	chr2:181988564-181988707	XLOC_001776
4	lnc-CERKL-2	chr2:181988623-181988706	NONHSAT075862
5	lnc-CERKL-2	chr2:182028673-182029275	NONHSAT075862
6	lnc-UBE2E3-1	chr2:181988562-181988707	XLOC_001776
7	lnc-CERKL-2	chr2:181991894-181992422	NONHSAT075862
8	lnc-CERKL-5	chr2:182029520-182030027	predAs_ge08_ITGA4_1
9	lnc-UBE2E3-1	chr2:181988659-181988707	XLOC_001776
10	lnc-UBE2E3-1	chr2:181988564-181988707	ENSG00000234663
11	lnc-UBE2E3-1	chr2:181976709-181976784	XLOC_001776
12	lnc-UBE2E3-1	chr2:181988623-181988707	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
TBPL1	miRNA target sites
MORF4L2	miRNA target sites
NAP1L2	miRNA target sites

Extended variants
information (count: 2276 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2276 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7569991	chr2:181975252-181975253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182378199	chr2:181975254-181975255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562015143	chr2:181975302-181975303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186719682	chr2:181975330-181975331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548232445	chr2:181975356-181975357	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs74565937	chr2:181975367-181975368	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529991798	chr2:181975382-181975383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546613196	chr2:181975439-181975440	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375462205	chr2:181975441-181975442	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566595520	chr2:181975450-181975451	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs565359165	chr2:181975451-181975452	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532598973	chr2:181975452-181975453	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547806205	chr2:181975496-181975497	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs569397567	chr2:181975556-181975557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140235409	chr2:181975562-181975563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555263167	chr2:181975601-181975602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575213065	chr2:181975628-181975629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7570421	chr2:181975639-181975640	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs73976807	chr2:181975664-181975665	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536840507	chr2:181975746-181975747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576856160	chr2:181975782-181975783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539301408	chr2:181975787-181975788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545606288	chr2:181975797-181975798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562698222	chr2:181975798-181975799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566040485	chr2:181975843-181975844	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs145303589	chr2:181975854-181975855	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs115628095	chr2:181975904-181975905	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs67542534	chr2:181975905-181975906	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs386391994	chr2:181975913-181975914	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs386391995	chr2:181975914-181975915	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs10674515	chr2:181975915-181975916	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs541628740	chr2:181975943-181975944	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs550738230	chr2:181976011-181976012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11335749	chr2:181976017-181976018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561621785	chr2:181976027-181976028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527596882	chr2:181976037-181976038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546574280	chr2:181976053-181976054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78045042	chr2:181976054-181976055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7355264	chr2:181976095-181976096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193136826	chr2:181976096-181976097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552433073	chr2:181976205-181976206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185657405	chr2:181976249-181976250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369713431	chr2:181976267-181976268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538005885	chr2:181976331-181976332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533104810	chr2:181976387-181976388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548819769	chr2:181976416-181976417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568734164	chr2:181976465-181976466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188554366	chr2:181976492-181976493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386653266	chr2:181976494-181976495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76245446	chr2:181976495-181976496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181972400-181976400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:181973800-181985000	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr2:181974000-181985200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr2:181974200-181980200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr2:181974600-181980800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:181975000-181975800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr2:181975200-181975400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:181975800-181976000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
9	chr2:181980000-181980800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr2:181980200-181981400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr2:181980800-181981000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr2:181980800-181981400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:181980800-181982800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:181981000-181981400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr2:181981000-181985000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr2:181981400-181982400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:181981400-181984800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr2:181981400-181988600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr2:181982400-181982600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr2:181982400-181982800	Enhancers	Stomach Mucosa	stomach
21	chr2:181982600-181982800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:181982600-181985200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr2:181982800-181985000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr2:181983200-181983600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:181983600-181988400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:181984200-181986000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr2:181984800-181985600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:181984800-181988200	Enhancers	Primary T cells from cord blood	blood
29	chr2:181985000-181985600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:181985000-181985800	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr2:181985000-181988400	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr2:181985000-181988800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:181985000-181990200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:181985200-181985800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr2:181985200-181985800	Enhancers	NH-A	brain
36	chr2:181985200-181987000	Enhancers	HSMMtube	muscle
37	chr2:181985200-181987800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr2:181985200-181988000	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr2:181985400-181985800	Enhancers	HMEC	breast
40	chr2:181985400-181986000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr2:181985400-181986400	Enhancers	HSMM	muscle
42	chr2:181985400-181986800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr2:181985600-181986600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr2:181985600-181988400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:181985800-181986200	Enhancers	Primary T cells fromperipheralblood	blood
46	chr2:181985800-181986800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:181985800-181987000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr2:181985800-181988400	Weak transcription	HMEC	breast
49	chr2:181985800-181988400	Weak transcription	NH-A	brain
50	chr2:181986000-181986800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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