Variant report

Variant	nsv974446
Chromosome Location	chr14:22203023-22210672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:22202784-22203163	Medullo	brain:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
2	CTCF	chr14:22202920-22203070	GM12874	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
3	CTCF	chr14:22202880-22203030	HPAF	blood vessel:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
4	CTCF	chr14:22202813-22203031	ECC-1	luminal epithelium:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
5	CTCF	chr14:22202880-22203030	GM12801	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
6	CTCF	chr14:22202829-22203063	GM10266	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
7	CTCF	chr14:22202900-22203050	HPF	lung:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
8	CTCF	chr14:22202880-22203030	Hela-S3	cervix:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
9	CTCF	chr14:22202880-22203030	GM06990	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
10	CTCF	chr14:22202582-22203312	SK-N-SH	brain:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
11	CTCF	chr14:22202813-22203061	LNCaP	prostate:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
12	CTCF	chr14:22202827-22203152	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
13	CTCF	chr14:22202880-22203030	GM12865	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
14	CTCF	chr14:22202793-22203083	MCF-7	breast:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
15	CTCF	chr14:22202831-22203039	SK-N-SH_RA	brain:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
16	CTCF	chr14:22202767-22203068	H1-hESC	embryonic stem cell:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
17	CTCF	chr14:22202880-22203030	GM12871	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
18	CTCF	chr14:22202900-22203050	HFF-Myc	foreskin:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
19	CTCF	chr14:22202828-22203068	Spleen_OC	spleen:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
20	CTCF	chr14:22202729-22203151	GM12878	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
21	CTCF	chr14:22202795-22203078	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
22	CTCF	chr14:22202868-22203040	Kidney_OC	kidney:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
23	CTCF	chr14:22202880-22203030	BE2_C	brain:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
24	CTCF	chr14:22202768-22203141	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
25	CTCF	chr14:22202880-22203030	AG09319	gingival:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
26	CTCF	chr14:22202900-22203050	HEEpiC	esophagus:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
27	CTCF	chr14:22202728-22203163	H1-hESC	embryonic stem cell:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
28	CTCF	chr14:22202980-22203130	A549	lung:	n/a	n/a
29	CTCF	chr14:22202900-22203050	GM12873	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
30	CTCF	chr14:22202849-22203023	GM10248	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
31	CTCF	chr14:22202940-22203090	GM12864	blood:	n/a	chr14:22202940-22202961
32	CTCF	chr14:22202900-22203050	GM12866	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
33	CTCF	chr14:22202880-22203030	MCF-7	breast:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
34	CTCF	chr14:22202800-22203079	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
35	CTCF	chr14:22202635-22203222	HCT-116	colon:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
36	CTCF	chr14:22202880-22203030	HMEC	breast:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
37	CTCF	chr14:22203140-22203290	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr14:22202798-22203050	GM13977	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
39	CTCF	chr14:22202768-22203039	A549	lung:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
40	CTCF	chr14:22202880-22203030	BJ	skin:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
41	CTCF	chr14:22202865-22203167	HCT-116	colon:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
42	CTCF	chr14:22202880-22203030	RPTEC	kidney:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
43	CTCF	chr14:22202960-22203110	HAc	cerebellar:	n/a	n/a
44	CTCF	chr14:22202900-22203050	HVMF	connective:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
45	CTCF	chr14:22202900-22203050	AoAF	blood vessel:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
46	CTCF	chr14:22202747-22203149	A549	lung:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
47	CTCF	chr14:22202880-22203030	NHEK	skin:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
48	CTCF	chr14:22203100-22203250	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr14:22202880-22203030	HRE	kidney:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
50	CTCF	chr14:22202697-22203134	HepG2	liver:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:22191619..22192367-chr14:22202463..22203027,2	MCF-7	breast:
2	chr14:22202912..22203435-chr14:22216852..22217387,2	MCF-7	breast:

Variant related genes	Relation type
TRAV4	TF binding region
ENSG00000211777	chromatin interactions

Extended variants
information (count: 316 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371399877	chr14:22203041-22203042	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs542417595	chr14:22203130-22203131	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs34576814	chr14:22203148-22203149	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs397853524	chr14:22203157-22203158	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs562352143	chr14:22203162-22203163	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs529741543	chr14:22203197-22203198	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546682143	chr14:22203222-22203223	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566318581	chr14:22203237-22203238	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553493995	chr14:22203244-22203245	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs532150964	chr14:22203251-22203252	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs556690968	chr14:22203258-22203259	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551792614	chr14:22203296-22203297	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12590415	chr14:22203306-22203307	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs12590420	chr14:22203345-22203346	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150761663	chr14:22203403-22203404	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs111885433	chr14:22203405-22203406	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs533991442	chr14:22203406-22203407	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs185887561	chr14:22203521-22203522	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs577129010	chr14:22203526-22203527	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145322202	chr14:22203562-22203563	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs78231430	chr14:22203606-22203607	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs114138928	chr14:22203616-22203617	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs542583695	chr14:22203683-22203684	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs562099757	chr14:22203716-22203717	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572602451	chr14:22203726-22203727	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs539916065	chr14:22203744-22203745	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs560180084	chr14:22203768-22203769	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs190866689	chr14:22203830-22203831	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs2320056	chr14:22203869-22203870	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562185027	chr14:22203887-22203888	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570491969	chr14:22203923-22203924	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs531462925	chr14:22203928-22203929	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548469530	chr14:22203962-22203963	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs568132432	chr14:22203970-22203971	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534004760	chr14:22204065-22204066	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs183263626	chr14:22204108-22204109	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs147216496	chr14:22204146-22204147	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs534704565	chr14:22204151-22204152	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs539985450	chr14:22204182-22204183	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs115892427	chr14:22204185-22204186	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370503658	chr14:22204199-22204200	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs536107160	chr14:22204243-22204244	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs553032190	chr14:22204272-22204273	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs140334349	chr14:22204282-22204283	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572685763	chr14:22204304-22204305	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs186383893	chr14:22204336-22204337	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs564571215	chr14:22204377-22204378	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576524746	chr14:22204382-22204383	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs545504956	chr14:22204390-22204391	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113037741	chr14:22204417-22204418	Weak transcription Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21364760	CNVD
Autism	22102821	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22188400-22209600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:22198600-22203200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr14:22202600-22203200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:22202600-22203200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr14:22202800-22203200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr14:22202800-22203200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
7	chr14:22202800-22203200	Active TSS	Brain Cingulate Gyrus	brain
8	chr14:22202800-22203200	Active TSS	Brain Substantia Nigra	brain
9	chr14:22203000-22203200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
10	chr14:22203000-22203200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr14:22203000-22203200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr14:22203000-22203200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:22203000-22203400	Active TSS	Brain Hippocampus Middle	brain
14	chr14:22203200-22203400	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr14:22203200-22203400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr14:22203200-22203400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:22203200-22204000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr14:22203200-22204000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:22203400-22205600	Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr14:22203800-22205200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr14:22203800-22205400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
22	chr14:22203800-22205800	Active TSS	Primary T cells from cord blood	blood
23	chr14:22204000-22204400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:22204000-22205200	Bivalent/Poised TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr14:22204000-22205800	Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr14:22204000-22206200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr14:22204000-22207000	Active TSS	Fetal Thymus	thymus
28	chr14:22204000-22208200	Active TSS	Thymus	Thymus
29	chr14:22204400-22204600	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:22204600-22204800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr14:22205400-22206600	Active TSS	Primary T cells fromperipheralblood	blood
32	chr14:22205600-22206000	Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr14:22205600-22208800	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
34	chr14:22205800-22206000	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
35	chr14:22205800-22207400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
36	chr14:22206000-22206400	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr14:22206200-22208000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr14:22206400-22206600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
39	chr14:22206600-22206800	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr14:22206600-22207000	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
41	chr14:22207000-22207200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr14:22207000-22211200	Active TSS	Primary T cells fromperipheralblood	blood
43	chr14:22208000-22208200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr14:22208000-22209000	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr14:22208200-22208400	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr14:22208200-22209400	Active TSS	Primary T cells from cord blood	blood
47	chr14:22208400-22208600	Bivalent/Poised TSS	Fetal Thymus	thymus
48	chr14:22208600-22209400	Active TSS	Fetal Thymus	thymus
49	chr14:22209000-22210200	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr14:22209400-22210600	Bivalent/Poised TSS	Primary T cells from cord blood	blood

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