Variant report

Variant	rs531583877
Chromosome Location	chr14:22382239-22382240
allele	C/G
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	RAD21	chr14:22381800-22382403	A549	lung:	n/a	chr14:22382116-22382135
2	CTCF	chr14:22381993-22382263	NHEK	skin:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
3	MAX	chr14:22381972-22382245	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr14:22382001-22382378	GM10248	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
5	CTCF	chr14:22381845-22382474	SK-N-SH	brain:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
6	CTCF	chr14:22381959-22382291	HepG2	liver:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
7	JUN	chr14:22382016-22382381	HUVEC	blood vessel:	n/a	chr14:22382200-22382208
8	CTCF	chr14:22381878-22382345	HepG2	liver:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
9	SMC3	chr14:22381981-22382303	HepG2	liver:	n/a	chr14:22382117-22382131
10	CTCF	chr14:22381977-22382246	A549	lung:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
11	CTCF	chr14:22382009-22382270	Fibrobl	skin:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
12	CTCF	chr14:22381990-22382250	K562	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
13	RAD21	chr14:22381981-22382302	SK-N-SH_RA	brain:	n/a	chr14:22382116-22382135
14	RAD21	chr14:22381911-22382332	H1-hESC	embryonic stem cell:	n/a	chr14:22382116-22382135
15	RAD21	chr14:22381985-22382320	A549	lung:	n/a	chr14:22382116-22382135
16	RAD21	chr14:22381898-22382388	MCF-7	breast:	n/a	chr14:22382116-22382135
17	CTCF	chr14:22381973-22382252	GM12878	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
18	CTCF	chr14:22381873-22382347	H1-hESC	embryonic stem cell:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
19	CTCF	chr14:22382072-22382253	GM12891	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
20	CTCF	chr14:22381941-22382325	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
21	CTCF	chr14:22381981-22382254	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
22	CTCF	chr14:22382014-22382252	LNCaP	prostate:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
23	CTCF	chr14:22382041-22382250	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
24	ZNF143	chr14:22381957-22382318	GM12878	blood:	n/a	n/a
25	CTCF	chr14:22382200-22382350	HAc	cerebellar:	n/a	n/a
26	FOSL2	chr14:22381909-22382442	A549	lung:	n/a	chr14:22382200-22382208
27	FOS	chr14:22382104-22382280	MCF10A-Er-Src	breast:	n/a	chr14:22382200-22382208 chr14:22382198-22382209
28	CTCF	chr14:22382140-22382290	GM12869	blood:	n/a	n/a
29	RAD21	chr14:22381922-22382353	HepG2	liver:	n/a	chr14:22382116-22382135
30	CTCF	chr14:22381941-22382314	K562	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
31	CTCF	chr14:22382028-22382330	Kidney_OC	kidney:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
32	CTCF	chr14:22382120-22382270	WI-38	lung:	n/a	n/a
33	CTCF	chr14:22381995-22382262	ProgFib	skin:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
34	CTCF	chr14:22381991-22382239	GM10266	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
35	CTCF	chr14:22381891-22382318	K562	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
36	CTCF	chr14:22382160-22382310	A549	lung:	n/a	n/a
37	NR3C1	chr14:22381985-22382364	A549	lung:	n/a	chr14:22382199-22382208
38	RAD21	chr14:22381954-22382377	ECC-1	luminal epithelium:	n/a	chr14:22382116-22382135
39	MXI1	chr14:22382010-22382269	HepG2	liver:	n/a	n/a
40	CTCF	chr14:22381983-22382281	Spleen_OC	spleen:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
41	CTCF	chr14:22381968-22382260	A549	lung:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
42	CTCF	chr14:22381980-22382243	GM19239	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
43	CTCF	chr14:22382036-22382258	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
44	RAD21	chr14:22381955-22382271	HepG2	liver:	n/a	chr14:22382116-22382135
45	CTCF	chr14:22381969-22382258	H1-hESC	embryonic stem cell:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
46	CTCF	chr14:22381853-22382432	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
47	CTCF	chr14:22381824-22382339	HCT-116	colon:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
48	CTCF	chr14:22381780-22382464	A549	lung:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
49	ZMIZ1	chr14:22382197-22382263	K562	blood:	n/a	n/a
50	CTCF	chr14:22382003-22382241	HepG2	liver:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138

No.	Distal block	Cell Line	Cell type
1	chr14:22381561..22382521-chr14:22456003..22456911,2	MCF-7	breast:
2	chr14:22355742..22356307-chr14:22381815..22382504,2	MCF-7	breast:
3	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
4	chr14:22381747..22382682-chr14:22568612..22569505,2	MCF-7	breast:
5	chr14:22381656..22382465-chr5:35444689..35445277,2	MCF-7	breast:

Variant related genes	Relation type
TRAV13-2	TF binding region
ENSG00000211789	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042309	chr14:22042511-22866936	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
2	nsv832741	chr14:22235781-22413637	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	esv3387723	chr14:22255284-22397765	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv430885	chr14:22267491-22975700	Enhancers Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	124 gene(s)	inside rSNPs	diseases
5	nsv524527	chr14:22288841-22387318	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv430886	chr14:22290777-22975700	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
7	nsv1045059	chr14:22299148-22911214	Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases
8	nsv916328	chr14:22299151-22793429	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
9	nsv430887	chr14:22299981-23069853	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	173 gene(s)	inside rSNPs	diseases
10	nsv832742	chr14:22307760-22501748	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv533184	chr14:22322590-22964922	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
12	esv3406578	chr14:22323357-22384327	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv430888	chr14:22328266-22974256	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	118 gene(s)	inside rSNPs	diseases
14	nsv826884	chr14:22329745-23005270	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	147 gene(s)	inside rSNPs	diseases
15	nsv826885	chr14:22329745-23005311	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	147 gene(s)	inside rSNPs	diseases
16	nsv826887	chr14:22330625-22998976	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	142 gene(s)	inside rSNPs	diseases
17	nsv430889	chr14:22338141-22988571	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	134 gene(s)	inside rSNPs	diseases
18	nsv430890	chr14:22349686-22970327	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
19	nsv1038915	chr14:22352968-22991087	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	135 gene(s)	inside rSNPs	diseases
20	nsv430892	chr14:22354103-22968854	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
21	nsv901482	chr14:22356551-22392983	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
22	nsv826888	chr14:22373770-23001710	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	140 gene(s)	inside rSNPs	diseases
23	nsv430893	chr14:22378542-22974256	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	114 gene(s)	inside rSNPs	diseases
24	nsv430894	chr14:22378542-22975700	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	115 gene(s)	inside rSNPs	diseases
25	nsv430895	chr14:22379160-22946380	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
26	nsv826889	chr14:22379803-23001761	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	139 gene(s)	inside rSNPs	diseases
27	nsv430896	chr14:22380824-22942619	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
28	nsv430897	chr14:22380824-22975700	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	115 gene(s)	inside rSNPs	diseases
29	nsv1048072	chr14:22381424-22394436	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
30	nsv430903	chr14:22381424-22913994	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
31	nsv430904	chr14:22381424-22968854	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	109 gene(s)	inside rSNPs	diseases
32	nsv430899	chr14:22381424-22974256	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	114 gene(s)	inside rSNPs	diseases
33	nsv430905	chr14:22382074-22970327	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	110 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22380200-22383200	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr14:22380400-22382400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr14:22380400-22382400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:22380400-22386200	Enhancers	HUVEC	blood vessel
5	chr14:22380600-22386600	Weak transcription	Gastric	stomach
6	chr14:22380800-22383400	Weak transcription	Primary B cells from cord blood	blood
7	chr14:22381600-22386200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr14:22381800-22382600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:22381800-22382800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr14:22381800-22382800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr14:22381800-22384400	Enhancers	Fetal Thymus	thymus
12	chr14:22381800-22386400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr14:22382000-22382400	Enhancers	Primary B cells from peripheral blood	blood
14	chr14:22382000-22382400	Enhancers	Primary T cells fromperipheralblood	blood
15	chr14:22382000-22382400	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr14:22382000-22382600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr14:22382000-22382600	Enhancers	Dnd41	blood
18	chr14:22382000-22382800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr14:22382000-22382800	Enhancers	Pancreas	Pancrea
20	chr14:22382000-22383200	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr14:22382000-22383600	Enhancers	A549	lung
22	chr14:22382000-22384200	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr14:22382000-22386600	Enhancers	Stomach Mucosa	stomach
24	chr14:22382200-22382400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:22382200-22382400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr14:22382200-22382400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr14:22382200-22382400	Enhancers	Liver	Liver
28	chr14:22382200-22382400	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr14:22382200-22382400	Enhancers	Brain Substantia Nigra	brain
30	chr14:22382200-22382400	Flanking Active TSS	Thymus	Thymus
31	chr14:22382200-22382400	Enhancers	HepG2	liver
32	chr14:22382200-22382600	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr14:22382200-22382800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:22382200-22383000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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