Variant report

Variant	rs466399
Chromosome Location	chr3:161091194-161091195
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GABPA	chr3:161089095-161091343	MCF-7	breast:	n/a	n/a
2	HDAC2	chr3:161089058-161091208	MCF-7	breast:	n/a	chr3:161089632-161089651
3	EP300	chr3:161089035-161091712	MCF-7	breast:	n/a	chr3:161089801-161089817
4	E2F6	chr3:161089363-161091367	H1-hESC	embryonic stem cell:	n/a	n/a
5	GTF2F1	chr3:161090465-161091202	H1-hESC	embryonic stem cell:	n/a	n/a
6	FOSL2	chr3:161089080-161091306	MCF-7	breast:	n/a	chr3:161090986-161090995
7	EGR1	chr3:161089059-161091222	MCF-7	breast:	n/a	chr3:161089796-161089809 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089416-161089438 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089420-161089434 chr3:161090857-161090864
8	JUND	chr3:161091104-161091242	H1-hESC	embryonic stem cell:	n/a	n/a
9	GABPA	chr3:161089048-161091265	MCF-7	breast:	n/a	n/a
10	ELF1	chr3:161089077-161091484	MCF-7	breast:	n/a	n/a
11	PML	chr3:161089034-161091298	MCF-7	breast:	n/a	n/a
12	TCF12	chr3:161088987-161091243	MCF-7	breast:	n/a	n/a
13	SIN3A	chr3:161089119-161091303	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAX	chr3:161089003-161091383	MCF-7	breast:	n/a	chr3:161089343-161089353
15	FOXM1	chr3:161089001-161091338	MCF-7	breast:	n/a	n/a
16	POLR2A	chr3:161088958-161091206	MCF-7	breast:	n/a	n/a
17	POLR2A	chr3:161089036-161091199	H1-hESC	embryonic stem cell:	n/a	n/a
18	TCF12	chr3:161088830-161091241	MCF-7	breast:	n/a	n/a
19	POLR2A	chr3:161084726-161091997	MCF-7	breast:	n/a	n/a
20	REST	chr3:161089041-161091357	MCF-7	breast:	n/a	n/a
21	POLR2A	chr3:161088984-161091224	ProgFib	skin:	n/a	n/a
22	MAX	chr3:161089022-161091279	MCF-7	breast:	n/a	chr3:161089343-161089353
23	TAF1	chr3:161088683-161091222	MCF-7	breast:	n/a	n/a
24	CEBPB	chr3:161089085-161091543	MCF-7	breast:	n/a	n/a
25	JUND	chr3:161088963-161091603	MCF-7	breast:	n/a	chr3:161090986-161090995
26	TEAD4	chr3:161089112-161091366	MCF-7	breast:	n/a	n/a
27	SIN3AK20	chr3:161088214-161091361	MCF-7	breast:	n/a	n/a
28	PML	chr3:161088156-161091509	MCF-7	breast:	n/a	n/a
29	SRF	chr3:161089046-161091437	MCF-7	breast:	n/a	chr3:161089343-161089353
30	GATA3	chr3:161088834-161091443	MCF-7	breast:	n/a	chr3:161089781-161089790 chr3:161090986-161090996
31	GATA3	chr3:161088930-161091398	MCF-7	breast:	n/a	chr3:161089781-161089790 chr3:161090986-161090996
32	ELF1	chr3:161089164-161091329	MCF-7	breast:	n/a	n/a
33	SIN3AK20	chr3:161088075-161091497	MCF-7	breast:	n/a	n/a
34	HDAC2	chr3:161089016-161091234	MCF-7	breast:	n/a	chr3:161089632-161089651
35	NR2F2	chr3:161088681-161091423	MCF-7	breast:	n/a	n/a
36	GATA3	chr3:161089226-161091307	MCF-7	breast:	n/a	chr3:161089781-161089790 chr3:161090986-161090996

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:161091175-161091225	PANC-1	pancreas:	n/a
2	chr3:161091175-161091225	GM12878	blood:	n/a
3	chr3:161091175-161091225	ECC-1	luminal epithelium:	n/a
4	chr3:161091175-161091225	HUVEC	blood vessel:	n/a
5	chr3:161091175-161091225	CMK	blood:	n/a
6	chr3:161091175-161091225	LNCaP	prostate:	n/a
7	chr3:161091175-161091225	T-47D	breast:	n/a
8	chr3:161091175-161091225	HRCEpiC	kidney:	n/a
9	chr3:161091175-161091225	HRPEpiC	eye:	n/a
10	chr3:161091175-161091225	HCPEpiC	choroid plexus:	n/a
11	chr3:161091175-161091225	ProgFib	skin:	n/a
12	chr3:161091175-161091225	NHBE	bronchial:	n/a
13	chr3:161091175-161091225	NB4	blood:	n/a
14	chr3:161091175-161091225	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:161091175-161091225	ovcar-3	ovarian:	n/a
16	chr3:161091175-161091225	BE2_C	brain:	n/a
17	chr3:161091175-161091225	BJ	skin:	n/a
18	chr3:161091175-161091225	HCF	heart:	n/a
19	chr3:161091175-161091225	Jurkat	blood:	n/a
20	chr3:161091175-161091225	HL-60	blood:	n/a
21	chr3:161091175-161091225	AG10803	skin:	n/a
22	chr3:161091175-161091225	K562	blood:	n/a
23	chr3:161091175-161091225	NH-A	brain:	n/a
24	chr3:161091175-161091225	Hela-S3	cervix:	n/a
25	chr3:161091175-161091225	H1-hESC	embryonic stem cell:	embryo
26	chr3:161091175-161091225	SK-N-SH_RA	brain:	n/a
27	chr3:161091175-161091225	GM12892	blood:	n/a
28	chr3:161091175-161091225	HCT-116	colon:	n/a
29	chr3:161091175-161091225	GM12891	blood:	n/a
30	chr3:161091175-161091225	AG09309	skin:	n/a
31	chr3:161091175-161091225	NHDF-neo	bronchial:	n/a
32	chr3:161091175-161091225	AG04450	lung:	fetal
33	chr3:161091175-161091225	HRE	kidney:	n/a
34	chr3:161091175-161091225	AG09319	gingival:	n/a
35	chr3:161091175-161091225	SKMC	muscle:	n/a
36	chr3:161091175-161091225	GM06990	blood:	n/a
37	chr3:161091175-161091225	GM19239	blood:	n/a
38	chr3:161091175-161091225	HepG2	liver:	n/a
39	chr3:161091175-161091225	HMEC	breast:	n/a
40	chr3:161091175-161091225	HCM	heart:	n/a
41	chr3:161091175-161091225	SAEC	small airway:	n/a
42	chr3:161091175-161091225	Caco-2	colon:	n/a
43	chr3:161091175-161091225	HIPEpiC	eye:	n/a
44	chr3:161091175-161091225	AoSMC	blood vessel:	n/a
45	chr3:161091175-161091225	HEK293	kidney:	embryo
46	chr3:161091175-161091225	A549	lung:	n/a
47	chr3:161091175-161091225	RPTEC	kidney:	n/a
48	chr3:161091175-161091225	MCF-7	breast:	n/a
49	chr3:161091175-161091225	IMR90	lung:	fetal
50	chr3:161091175-161091225	HNPCEpiC	eye:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:161089815..161091859-chr5:87970263..87972091,2	MCF-7	breast:
2	chr3:161038392..161046344-chr3:161085640..161093564,25	MCF-7	breast:
3	chr3:160934982..160947568-chr3:161079696..161093037,40	MCF-7	breast:
4	chr3:161090661..161092175-chr9:130953250..130955416,2	MCF-7	breast:
5	chr20:45982415..45984680-chr3:161089076..161091449,2	MCF-7	breast:
6	chr3:160936365..160960187-chr3:161078472..161094658,51	MCF-7	breast:
7	chr11:75061761..75064404-chr3:161090947..161092751,2	MCF-7	breast:
8	chr3:161090533..161094064-chr8:101963094..101965869,3	MCF-7	breast:
9	chr3:161089431..161091438-chr6:26196434..26199354,2	MCF-7	breast:
10	chr17:57916984..57919121-chr3:161089806..161091709,2	MCF-7	breast:
11	chr3:161089882..161091893-chr9:14313286..14315891,2	MCF-7	breast:
12	chr3:160282384..160284279-chr3:161090070..161092453,3	MCF-7	breast:
13	chr11:65265519..65268230-chr3:161089523..161091817,2	MCF-7	breast:
14	chr3:160813033..160824577-chr3:161083489..161092050,35	MCF-7	breast:
15	chr3:160472518..160475131-chr3:161089184..161091851,3	MCF-7	breast:
16	chr14:38061358..38063507-chr3:161089489..161091930,2	MCF-7	breast:
17	chr21:46347538..46349062-chr3:161090013..161091580,2	MCF-7	breast:
18	chr17:57913968..57916411-chr3:161089503..161091564,2	MCF-7	breast:
19	chr22:30683032..30685513-chr3:161089094..161092006,2	MCF-7	breast:
20	chr20:56282039..56284863-chr3:161089358..161091881,2	MCF-7	breast:
21	chr3:160166836..160169216-chr3:161090028..161092220,2	MCF-7	breast:
22	chr3:161088340..161091318-chr9:131938931..131941651,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPTSSB	TF binding region
SPTSSB	CpG island
ENSG00000260572	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000124225	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000239282	Chromatin interaction
ENSG00000164924	Chromatin interaction
ENSG00000271052	Chromatin interaction
ENSG00000240138	Chromatin interaction
ENSG00000213186	Chromatin interaction
ENSG00000169251	Chromatin interaction
ENSG00000169255	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000188483	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000137486	Chromatin interaction
ENSG00000186432	Chromatin interaction
ENSG00000160255	Chromatin interaction
ENSG00000163590	Chromatin interaction
ENSG00000204055	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000148337	Chromatin interaction
ENSG00000147862	Chromatin interaction
ENSG00000245864	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000229320	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10804790	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1382427	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1382428	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1478565	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1600209	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs163328	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs189270	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1993891	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2404340	0.86[EUR][1000 genomes]
rs28515190	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs336541	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336543	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336548	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336549	0.81[EUR][1000 genomes]
rs336567	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336568	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs336569	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336570	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336572	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs336577	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336579	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336580	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs336582	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs336583	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336585	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336586	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336589	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336590	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336591	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs336593	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs339101	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3849524	0.88[EUR][1000 genomes]
rs4273380	0.83[EUR][1000 genomes]
rs4350933	0.85[EUR][1000 genomes]
rs4370045	0.82[EUR][1000 genomes]
rs4493448	0.84[EUR][1000 genomes]
rs455386	0.84[EUR][1000 genomes]
rs456611	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs457272	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs459515	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs459697	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4597724	0.85[EUR][1000 genomes]
rs460165	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460508	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs461638	0.84[EUR][1000 genomes]
rs462413	0.84[EUR][1000 genomes]
rs462514	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs463928	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs464766	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs465985	0.85[EUR][1000 genomes]
rs62279921	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6441373	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6762645	0.84[EUR][1000 genomes]
rs6765269	0.84[EUR][1000 genomes]
rs6775627	0.85[EUR][1000 genomes]
rs6794601	0.83[EUR][1000 genomes]
rs7615592	0.86[EUR][1000 genomes]
rs7623206	0.86[EUR][1000 genomes]
rs7629987	0.86[EUR][1000 genomes]
rs7638668	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7647327	0.88[EUR][1000 genomes]
rs7653233	0.87[EUR][1000 genomes]
rs7653361	0.87[EUR][1000 genomes]
rs9290073	0.82[EUR][1000 genomes]
rs9290074	0.86[EUR][1000 genomes]
rs975323	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9790314	0.88[EUR][1000 genomes]
rs9821201	0.88[EUR][1000 genomes]
rs9846756	0.85[EUR][1000 genomes]
rs9850455	0.88[EUR][1000 genomes]
rs9863590	0.83[EUR][1000 genomes]
rs9870059	0.88[EUR][1000 genomes]
rs9872514	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv877710	chr3:161087857-161245414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161088000-161091400	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr3:161089200-161091200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:161089200-161091200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
4	chr3:161089200-161091200	Active TSS	Brain Angular Gyrus	brain
5	chr3:161089200-161091200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
6	chr3:161089600-161091200	Active TSS	Fetal Brain Female	brain
7	chr3:161089600-161091200	Flanking Active TSS	Stomach Smooth Muscle	stomach
8	chr3:161090200-161091200	Active TSS	Fetal Brain Male	brain
9	chr3:161090400-161091200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr3:161090600-161091200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:161090600-161091200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
12	chr3:161090600-161091200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
13	chr3:161090600-161091200	Flanking Active TSS	Brain Anterior Caudate	brain
14	chr3:161090600-161091200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
15	chr3:161090600-161091200	Bivalent Enhancer	Fetal Heart	heart
16	chr3:161090600-161091200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
17	chr3:161090800-161091200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
18	chr3:161090800-161091200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
19	chr3:161090800-161091200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr3:161090800-161091200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:161090800-161091200	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr3:161090800-161091200	Enhancers	Gastric	stomach
23	chr3:161090800-161091200	Flanking Active TSS	Stomach Mucosa	stomach
24	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
25	chr3:161091000-161091200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr3:161091000-161091200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
27	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
28	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:161091000-161091200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr3:161091000-161091200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr3:161091000-161091200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr3:161091000-161091200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:161091000-161091200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:161091000-161091200	Bivalent Enhancer	Liver	Liver
37	chr3:161091000-161091200	Flanking Active TSS	Brain Cingulate Gyrus	brain
38	chr3:161091000-161091200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
39	chr3:161091000-161091200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:161091000-161091200	Enhancers	Brain Substantia Nigra	brain
41	chr3:161091000-161091200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
42	chr3:161091000-161091200	Bivalent Enhancer	Fetal Intestine Large	intestine
43	chr3:161091000-161091200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
44	chr3:161091000-161091200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
45	chr3:161091000-161091200	Active TSS	Right Ventricle	heart
46	chr3:161091000-161091800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood

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