Variant report

Variant	rs10148682
Chromosome Location	chr14:21738546-21738547
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	CREB1	chr14:21736959-21738568	HepG2	liver:	n/a	n/a
2	MYBL2	chr14:21735757-21738673	HepG2	liver:	n/a	chr14:21737687-21737701
3	BRCA1	chr14:21737406-21738551	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr14:21736942-21738549	HepG2	liver:	n/a	n/a
5	CHD1	chr14:21734912-21738567	IMR90	lung:	n/a	n/a
6	ZNF384	chr14:21737525-21738672	GM12878	blood:	n/a	n/a
7	POLR2A	chr14:21737810-21738563	HL-60	blood:	n/a	n/a
8	REST	chr14:21736324-21738570	H1-neurons	neurons:	n/a	n/a
9	POLR2A	chr14:21735190-21738569	GM12891	blood:	n/a	n/a
10	PBX3	chr14:21736950-21738562	SK-N-SH	brain:	n/a	chr14:21737913-21737933 chr14:21737824-21737833
11	GABPA	chr14:21737356-21738607	HL-60	blood:	n/a	chr14:21737994-21738003
12	USF2	chr14:21737570-21738546	Hela-S3	cervix:	n/a	n/a
13	MAX	chr14:21736358-21738623	A549	lung:	n/a	chr14:21736997-21737006
14	POLR2A	chr14:21735370-21738563	GM12878	blood:	n/a	n/a
15	E2F6	chr14:21737354-21738571	A549	lung:	n/a	chr14:21738069-21738086 chr14:21737994-21738006 chr14:21737994-21738003 chr14:21738076-21738083 chr14:21738076-21738083 chr14:21738226-21738235 chr14:21738076-21738083 chr14:21738069-21738086 chr14:21737911-21737920
16	ZKSCAN1	chr14:21737167-21738570	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr14:21738343-21738548	GM12878	blood:	n/a	n/a
18	NFIC	chr14:21735252-21738638	GM12878	blood:	n/a	n/a
19	POLR2A	chr14:21736298-21738760	SK-N-MC	brain:	n/a	n/a
20	PML	chr14:21736507-21738634	GM12878	blood:	n/a	chr14:21737514-21737522
21	GABPA	chr14:21737028-21738569	MCF-7	breast:	n/a	chr14:21737994-21738003
22	BCLAF1	chr14:21737799-21738615	GM12878	blood:	n/a	chr14:21738216-21738225 chr14:21737990-21738003
23	POLR2A	chr14:21737908-21738556	GM12891	blood:	n/a	n/a
24	POLR2A	chr14:21736423-21738550	GM12892	blood:	n/a	n/a
25	FOXM1	chr14:21736807-21738587	GM12878	blood:	n/a	n/a
26	POLR2A	chr14:21731378-21738564	GM12878	blood:	n/a	n/a
27	POLR2A	chr14:21736787-21738586	HL-60	blood:	n/a	n/a
28	SIN3AK20	chr14:21735442-21738552	MCF-7	breast:	n/a	n/a
29	MAX	chr14:21736368-21738647	HepG2	liver:	n/a	chr14:21736997-21737006
30	POLR2A	chr14:21737902-21738573	GM12892	blood:	n/a	n/a
31	TFAP2C	chr14:21737667-21738559	Hela-S3	cervix:	n/a	chr14:21738048-21738063
32	RUNX3	chr14:21736844-21738608	GM12878	blood:	n/a	n/a
33	POLR2A	chr14:21737866-21738579	PFSK-1	brain:	n/a	n/a
34	HCFC1	chr14:21735555-21738667	Hela-S3	cervix:	n/a	n/a
35	HEY1	chr14:21737891-21738591	HepG2	liver:	n/a	chr14:21737987-21738002
36	ELF1	chr14:21737253-21738572	MCF-7	breast:	n/a	chr14:21737978-21737991 chr14:21737888-21737899
37	MTA3	chr14:21737819-21738695	GM12878	blood:	n/a	n/a
38	POLR2A	chr14:21736422-21738549	GM19099	blood:	n/a	n/a
39	MAX	chr14:21736407-21738548	A549	lung:	n/a	chr14:21736997-21737006
40	ZNF384	chr14:21737518-21738579	K562	blood:	n/a	n/a
41	MBD4	chr14:21737893-21738586	HepG2	liver:	n/a	n/a
42	TFAP2A	chr14:21737909-21738560	Hela-S3	cervix:	n/a	chr14:21738366-21738377 chr14:21738053-21738061 chr14:21738366-21738377 chr14:21738053-21738061 chr14:21738362-21738377 chr14:21738053-21738061 chr14:21738366-21738377 chr14:21738366-21738377
43	GABPA	chr14:21737076-21738615	MCF-7	breast:	n/a	chr14:21737994-21738003
44	SPI1	chr14:21738046-21738616	HL-60	blood:	n/a	chr14:21738216-21738225 chr14:21738337-21738350 chr14:21738336-21738349
45	SPI1	chr14:21737787-21738667	GM12878	blood:	n/a	chr14:21738216-21738225 chr14:21738337-21738350 chr14:21738336-21738349
46	POLR2A	chr14:21735268-21738568	GM12878	blood:	n/a	n/a
47	MAX	chr14:21736360-21738553	MCF-7	breast:	n/a	chr14:21736997-21737006
48	GABPA	chr14:21737375-21738597	A549	lung:	n/a	chr14:21737994-21738003
49	SPI1	chr14:21738041-21738582	GM12891	blood:	n/a	chr14:21738216-21738225 chr14:21738337-21738350 chr14:21738336-21738349
50	MXI1	chr14:21735386-21738614	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21731892..21738562-chr14:21850801..21854193,10	MCF-7	breast:
2	chr14:21738165..21739837-chr14:21745511..21747672,2	K562	blood:
3	chr14:21736080..21739636-chr14:21765775..21769584,7	MCF-7	breast:
4	chr1:151429381..151432201-chr14:21736244..21738881,2	MCF-7	breast:
5	chr14:21736489..21738626-chr14:21851688..21853909,3	K562	blood:
6	chr14:21737121..21738626-chr14:21850627..21853188,2	K562	blood:

Variant related genes	Relation type
HNRNPC	TF binding region
ENSG00000092200	Chromatin interaction
ENSG00000260830	Chromatin interaction
ENSG00000092201	Chromatin interaction
ENSG00000143442	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10133539	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10142669	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10142891	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10145423	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148961	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10149383	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150916	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846887	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848128	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848510	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11849527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11849571	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850109	1.00[AMR][1000 genomes]
rs17092556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102606	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102889	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17103007	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1957415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28510166	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28609318	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8014450	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8016283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8016287	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9322956	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv901477	chr14:21625262-21750308	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv901478	chr14:21626497-21750308	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv541980	chr14:21672540-21742729	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
16	nsv541983	chr14:21676221-21742729	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
17	esv1825348	chr14:21691941-21829404	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
18	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
20	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
21	nsv541987	chr14:21692703-21742729	Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
22	nsv541989	chr14:21696056-21742729	Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
23	nsv541990	chr14:21702771-21757737	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
25	nsv983804	chr14:21730434-21759672	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21734000-21738600	Active TSS	Psoas Muscle	Psoas
2	chr14:21734800-21738600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:21736200-21738600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:21736200-21738600	Active TSS	Brain Angular Gyrus	brain
5	chr14:21737000-21738600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:21737800-21738600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
7	chr14:21737800-21738600	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr14:21737800-21738600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:21737800-21738600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr14:21737800-21738600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr14:21737800-21738600	Enhancers	Placenta	Placenta
12	chr14:21737800-21739000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr14:21737800-21743400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:21738000-21738600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:21738000-21738600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr14:21738000-21738600	Flanking Active TSS	Primary B cells from peripheral blood	blood
17	chr14:21738000-21738600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr14:21738000-21738600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr14:21738000-21738600	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr14:21738000-21738600	Flanking Active TSS	Fetal Intestine Small	intestine
21	chr14:21738000-21738600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
22	chr14:21738000-21738600	Flanking Active TSS	Rectal Smooth Muscle	rectum
23	chr14:21738000-21738600	Flanking Active TSS	Dnd41	blood
24	chr14:21738000-21738600	Flanking Active TSS	Hela-S3	cervix
25	chr14:21738200-21738600	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr14:21738200-21738600	Enhancers	Primary T cells from cord blood	blood
27	chr14:21738200-21738600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr14:21738200-21738600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:21738200-21738600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:21738200-21738600	Flanking Active TSS	Liver	Liver
31	chr14:21738200-21738600	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr14:21738200-21738600	Flanking Active TSS	Brain Cingulate Gyrus	brain
33	chr14:21738200-21738600	Enhancers	Fetal Heart	heart
34	chr14:21738200-21738600	Enhancers	Pancreas	Pancrea
35	chr14:21738200-21738600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr14:21738200-21738600	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr14:21738200-21738600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr14:21738200-21738600	Enhancers	Stomach Mucosa	stomach
39	chr14:21738200-21738600	Flanking Active TSS	Thymus	Thymus
40	chr14:21738200-21738600	Flanking Active TSS	A549	lung
41	chr14:21738200-21738600	Flanking Active TSS	GM12878-XiMat	blood
42	chr14:21738200-21738600	Flanking Active TSS	K562	blood
43	chr14:21738200-21738800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:21738400-21738600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr14:21738400-21738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:21738400-21738600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr14:21738400-21738600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr14:21738400-21738600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:21738400-21738600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:21738400-21738600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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