Variant report

Variant	nsv879860
Chromosome Location	chr4:122030864-122126808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:612)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:122037268-122037287	K562	blood:	n/a	n/a
2	ARID3A	chr4:122113614-122113950	HepG2	liver:	n/a	n/a
3	ATF2	chr4:122089668-122090578	GM12878	blood:	n/a	n/a
4	ATF2	chr4:122089650-122090546	GM12878	blood:	n/a	n/a
5	ATF2	chr4:122060489-122061174	GM12878	blood:	n/a	n/a
6	ATF2	chr4:122059076-122059639	GM12878	blood:	n/a	n/a
7	ATF2	chr4:122075100-122075725	GM12878	blood:	n/a	n/a
8	ATF2	chr4:122121054-122122668	GM12878	blood:	n/a	n/a
9	ATF2	chr4:122121135-122122529	GM12878	blood:	n/a	n/a
10	ATF2	chr4:122060584-122061213	GM12878	blood:	n/a	n/a
11	BACH1	chr4:122078182-122078402	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:122060596-122061029	GM12878	blood:	n/a	n/a
13	BATF	chr4:122035974-122036161	GM12878	blood:	n/a	n/a
14	BATF	chr4:122121892-122122296	GM12878	blood:	n/a	n/a
15	BATF	chr4:122034868-122035147	GM12878	blood:	n/a	n/a
16	BATF	chr4:122121069-122121846	GM12878	blood:	n/a	n/a
17	BATF	chr4:122060607-122060910	GM12878	blood:	n/a	n/a
18	BATF	chr4:122121244-122121725	GM12878	blood:	n/a	n/a
19	BATF	chr4:122059185-122059476	GM12878	blood:	n/a	n/a
20	BATF	chr4:122107036-122107324	GM12878	blood:	n/a	n/a
21	BATF	chr4:122089927-122090565	GM12878	blood:	n/a	n/a
22	BATF	chr4:122089894-122090503	GM12878	blood:	n/a	n/a
23	BATF	chr4:122034829-122035185	GM12878	blood:	n/a	n/a
24	BATF	chr4:122075266-122075602	GM12878	blood:	n/a	n/a
25	BATF	chr4:122121862-122122524	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:122089904-122090533	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:122121858-122122480	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:122060574-122061081	GM12878	blood:	n/a	chr4:122060918-122060927
29	BCL11A	chr4:122121433-122121728	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:122107128-122107466	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:122034863-122035206	GM12878	blood:	n/a	chr4:122035045-122035054
32	BCL11A	chr4:122107052-122107338	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:122121190-122121782	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:122090029-122090461	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:122121961-122122304	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:122060713-122060968	GM12878	blood:	n/a	chr4:122060918-122060927
37	BCL3	chr4:122121120-122121827	GM12878	blood:	n/a	n/a
38	BCL3	chr4:122121963-122122411	GM12878	blood:	n/a	n/a
39	BCL3	chr4:122059167-122059526	GM12878	blood:	n/a	n/a
40	BCL3	chr4:122089982-122090494	GM12878	blood:	n/a	n/a
41	BCLAF1	chr4:122121816-122122508	GM12878	blood:	n/a	n/a
42	BCLAF1	chr4:122121106-122122385	GM12878	blood:	n/a	n/a
43	BCLAF1	chr4:122089963-122090524	GM12878	blood:	n/a	n/a
44	BCLAF1	chr4:122089922-122090543	GM12878	blood:	n/a	n/a
45	BCLAF1	chr4:122060491-122061118	GM12878	blood:	n/a	chr4:122060918-122060927
46	BHLHE40	chr4:122106955-122107521	GM12878	blood:	n/a	chr4:122107182-122107195 chr4:122107185-122107194
47	BHLHE40	chr4:122060730-122060931	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:122121186-122122336	GM12878	blood:	n/a	n/a
49	BHLHE40	chr4:122090015-122090470	GM12878	blood:	n/a	n/a
50	CEBPB	chr4:122055322-122055333	HepG2	liver:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122059692-122059742	HRCEpiC	kidney:	n/a
2	chr4:122099598-122099648	H1-hESC	embryonic stem cell:	embryo
3	chr4:122059692-122059742	HRCEpiC	kidney:	n/a
4	chr4:122099598-122099648	H1-hESC	embryonic stem cell:	embryo
5	chr4:122086177-122086227	Jurkat	blood:	n/a
6	chr4:122078167-122078217	HRE	kidney:	n/a
7	chr4:122099598-122099648	HMEC	breast:	n/a
8	chr4:122059692-122059742	GM12891	blood:	n/a
9	chr4:122099598-122099648	T-47D	breast:	n/a
10	chr4:122110906-122110956	CMK	blood:	n/a
11	chr4:122059692-122059742	GM12878	blood:	n/a
12	chr4:122059692-122059742	SK-N-MC	brain:	n/a
13	chr4:122099598-122099648	AG10803	skin:	n/a
14	chr4:122053520-122053570	HRE	kidney:	n/a
15	chr4:122086137-122086187	HEK293	kidney:	embryo
16	chr4:122099598-122099648	HEEpiC	esophagus:	n/a
17	chr4:122110906-122110956	PrEC	prostate:	n/a
18	chr4:122085241-122085291	BE2_C	brain:	n/a
19	chr4:122053520-122053570	LNCaP	prostate:	n/a
20	chr4:122110906-122110956	NHDF-neo	bronchial:	n/a
21	chr4:122110906-122110956	HCM	heart:	n/a
22	chr4:122099598-122099648	HCT-116	colon:	n/a
23	chr4:122078348-122078398	HepG2	liver:	n/a
24	chr4:122059692-122059742	HCM	heart:	n/a
25	chr4:122078348-122078398	PFSK-1	brain:	n/a
26	chr4:122078348-122078398	HMEC	breast:	n/a
27	chr4:122059692-122059742	ProgFib	skin:	n/a
28	chr4:122085241-122085291	PFSK-1	brain:	n/a
29	chr4:122078167-122078217	SK-N-SH_RA	brain:	n/a
30	chr4:122085241-122085291	NT2-D1	testis:	n/a
31	chr4:122086177-122086227	HCM	heart:	n/a
32	chr4:122086137-122086187	PFSK-1	brain:	n/a
33	chr4:122078348-122078398	HL-60	blood:	n/a
34	chr4:122099598-122099648	ProgFib	skin:	n/a
35	chr4:122086698-122086748	SK-N-SH	brain:	n/a
36	chr4:122059692-122059742	LNCaP	prostate:	n/a
37	chr4:122059692-122059742	BJ	skin:	n/a
38	chr4:122059692-122059742	GM12892	blood:	n/a
39	chr4:122053520-122053570	HUVEC	blood vessel:	n/a
40	chr4:122085241-122085291	GM12891	blood:	n/a
41	chr4:122085241-122085291	MCF10A-Er-Src	breast:	n/a
42	chr4:122086177-122086227	HCT-116	colon:	n/a
43	chr4:122059692-122059742	SK-N-SH_RA	brain:	n/a
44	chr4:122085241-122085291	U87	brain:	n/a
45	chr4:122086698-122086748	AG04449	skin:	fetal
46	chr4:122053520-122053570	HNPCEpiC	eye:	n/a
47	chr4:122085241-122085291	Caco-2	colon:	n/a
48	chr4:122099598-122099648	ovcar-3	ovarian:	n/a
49	chr4:122086177-122086227	SK-N-MC	brain:	n/a
50	chr4:122078167-122078217	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:122120724..122123335-chr4:122133956..122135681,2	MCF-7	breast:
2	chr4:122093188..122094805-chr4:122094837..122097333,2	K562	blood:
3	chr4:122071769..122073481-chr4:122078376..122080913,2	K562	blood:
4	chr4:122096744..122098475-chr4:122101573..122104186,2	MCF-7	breast:
5	chr4:122096744..122098475-chr4:122101573..122104186,2	MCF-7	breast:
6	chr4:122093188..122094805-chr4:122094837..122097333,2	K562	blood:
7	chr4:122113303..122113806-chr4:122173095..122173613,2	K562	blood:
8	chr4:122113451..122113992-chr4:122228663..122229475,2	K562	blood:
9	chr4:122059912..122061901-chr4:122070461..122073391,2	MCF-7	breast:
10	chr4:122112861..122113764-chr4:122195514..122196479,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC079341.1-8	chr4:122062548-122064208	predAs_engstrom06_BC030136_1
2	lnc-AC079341.1-9	chr4:122039454-122039889	NONHSAT098136

No data

Variant related genes	Relation type
TNIP3	TF binding region
ENSG00000271302	TF binding region
RNU6-948P	TF binding region
TNIP3	CpG island
ENSG00000271302	CpG island
RNU6-948P	CpG island
ENSG00000050730	chromatin interactions

Extended variants
information (count: 3662 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3662 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6833755	chr4:122030864-122030865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556473137	chr4:122030865-122030866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566465380	chr4:122030886-122030887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575726473	chr4:122030997-122030998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537826386	chr4:122031132-122031133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114456778	chr4:122031141-122031142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578005418	chr4:122031179-122031180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1511095	chr4:122031206-122031207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560363415	chr4:122031209-122031210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370582159	chr4:122031243-122031244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374837564	chr4:122031248-122031249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564869469	chr4:122031263-122031264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560767008	chr4:122031279-122031280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151322575	chr4:122031305-122031306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115564284	chr4:122031336-122031337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141005568	chr4:122031357-122031358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528912656	chr4:122031368-122031369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140461867	chr4:122031373-122031374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562575194	chr4:122031383-122031384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186286527	chr4:122031389-122031390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558441531	chr4:122031455-122031456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564999579	chr4:122031458-122031459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527432828	chr4:122031470-122031471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74425225	chr4:122031505-122031506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547510325	chr4:122031547-122031548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567494469	chr4:122031548-122031549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536433108	chr4:122031573-122031574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189872955	chr4:122031599-122031600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182145521	chr4:122031616-122031617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538249945	chr4:122031624-122031625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557909114	chr4:122031641-122031642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551173126	chr4:122031656-122031657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534062100	chr4:122031671-122031672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553833250	chr4:122031678-122031679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571837680	chr4:122031759-122031760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557125961	chr4:122031792-122031793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116753531	chr4:122031821-122031822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573858915	chr4:122031904-122031905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187250085	chr4:122031935-122031936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562845973	chr4:122031938-122031939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114784372	chr4:122031967-122031968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367942321	chr4:122031984-122031985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545673385	chr4:122031996-122031997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564772642	chr4:122032051-122032052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116636625	chr4:122032145-122032146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149983301	chr4:122032189-122032190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534104754	chr4:122032190-122032191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76052099	chr4:122032200-122032201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192868126	chr4:122032282-122032283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574475530	chr4:122032322-122032323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122025200-122039200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr4:122030000-122034000	Weak transcription	Primary T cells from cord blood	blood
3	chr4:122034000-122034200	Enhancers	Primary T cells from cord blood	blood
4	chr4:122034200-122035000	Weak transcription	Primary T cells from cord blood	blood
5	chr4:122034400-122035200	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr4:122034600-122035800	Enhancers	GM12878-XiMat	blood
7	chr4:122035000-122035600	Enhancers	Primary T cells from cord blood	blood
8	chr4:122035000-122036200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:122035200-122039600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr4:122035600-122039200	Weak transcription	Primary T cells from cord blood	blood
11	chr4:122039200-122039400	Enhancers	Fetal Thymus	thymus
12	chr4:122039200-122040000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr4:122039200-122040800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr4:122039200-122041200	Enhancers	Primary T cells from cord blood	blood
15	chr4:122039400-122040800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr4:122039400-122040800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr4:122039600-122040000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr4:122039600-122040200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr4:122039600-122040600	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr4:122039600-122041000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr4:122040200-122041000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr4:122040800-122047400	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr4:122041000-122050800	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr4:122041200-122046200	Weak transcription	Primary T cells from cord blood	blood
25	chr4:122044000-122044200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:122044000-122044400	Enhancers	HSMM	muscle
27	chr4:122046200-122047000	Enhancers	HepG2	liver
28	chr4:122046200-122048600	Enhancers	Primary T cells from cord blood	blood
29	chr4:122047400-122047600	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr4:122047600-122050600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr4:122048600-122050600	Weak transcription	Primary T cells from cord blood	blood
32	chr4:122050600-122051600	Enhancers	Primary T cells from cord blood	blood
33	chr4:122050600-122051600	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr4:122050600-122051600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr4:122050800-122051400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr4:122050800-122051600	Enhancers	Primary T cells fromperipheralblood	blood
37	chr4:122050800-122051600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr4:122050800-122051600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr4:122050800-122051800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr4:122050800-122051800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr4:122050800-122052000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr4:122051000-122051200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:122051200-122052000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:122051600-122053000	Weak transcription	Primary T cells from cord blood	blood
45	chr4:122051600-122055800	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr4:122051600-122055800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr4:122051600-122059000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr4:122051600-122059400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr4:122051800-122055800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr4:122051800-122055800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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