Variant report

Variant	rs659424
Chromosome Location	chr19:56637491-56637492
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr19:56637068-56637665	K562	blood:	n/a	n/a
2	STAT5A	chr19:56637186-56637616	K562	blood:	n/a	n/a
3	MEF2A	chr19:56637151-56637621	K562	blood:	n/a	n/a
4	RCOR1	chr19:56637077-56637805	K562	blood:	n/a	n/a
5	E2F6	chr19:56637255-56637529	K562	blood:	n/a	chr19:56637340-56637350
6	GABPA	chr19:56637151-56637621	K562	blood:	n/a	n/a
7	TBL1XR1	chr19:56637105-56637630	K562	blood:	n/a	n/a
8	POLR2A	chr19:56637212-56637551	K562	blood:	n/a	n/a
9	GTF2B	chr19:56637280-56637496	K562	blood:	n/a	n/a
10	PML	chr19:56637214-56637683	K562	blood:	n/a	n/a
11	GATA1	chr19:56637279-56637703	PBDEFetal	blood:	n/a	n/a
12	BHLHE40	chr19:56636955-56637690	K562	blood:	n/a	chr19:56637336-56637352
13	CCNT2	chr19:56637255-56637615	K562	blood:	n/a	n/a
14	CEBPB	chr19:56637357-56637606	K562	blood:	n/a	n/a
15	GATA2	chr19:56637194-56637640	K562	blood:	n/a	n/a
16	MYC	chr19:56637149-56637629	K562	blood:	n/a	n/a
17	EP300	chr19:56637267-56637573	K562	blood:	n/a	n/a
18	MAX	chr19:56637151-56637620	K562	blood:	n/a	n/a
19	POLR2A	chr19:56637234-56637678	K562	blood:	n/a	n/a
20	TRIM28	chr19:56637196-56637716	K562	blood:	n/a	n/a
21	GATA1	chr19:56636885-56637838	PBDE	blood:	n/a	n/a
22	ELF1	chr19:56637145-56637504	K562	blood:	n/a	n/a
23	TBL1XR1	chr19:56637079-56637588	K562	blood:	n/a	n/a
24	TEAD4	chr19:56637065-56637724	K562	blood:	n/a	n/a
25	EP300	chr19:56637165-56637620	K562	blood:	n/a	n/a
26	TEAD4	chr19:56637082-56637560	K562	blood:	n/a	n/a
27	UBTF	chr19:56637127-56637567	K562	blood:	n/a	n/a
28	ETS1	chr19:56637239-56637500	K562	blood:	n/a	n/a
29	MAX	chr19:56637212-56637570	K562	blood:	n/a	n/a
30	ATF1	chr19:56637165-56637578	K562	blood:	n/a	n/a
31	CEBPD	chr19:56637201-56637688	K562	blood:	n/a	n/a
32	MYC	chr19:56637190-56637653	K562	blood:	n/a	n/a
33	POLR2A	chr19:56637242-56637544	K562	blood:	n/a	n/a
34	GATA2	chr19:56637043-56637624	K562	blood:	n/a	n/a
35	STAT5A	chr19:56637155-56637702	K562	blood:	n/a	chr19:56637163-56637172 chr19:56637164-56637173
36	KAP1	chr19:56637152-56637541	K562	blood:	n/a	n/a
37	POLR2A	chr19:56637153-56637584	K562	blood:	n/a	n/a
38	CUX1	chr19:56637260-56637640	K562	blood:	n/a	n/a
39	RCOR1	chr19:56637126-56637668	K562	blood:	n/a	n/a
40	REST	chr19:56637217-56637575	K562	blood:	n/a	n/a
41	JUND	chr19:56637127-56637700	K562	blood:	n/a	n/a
42	MXI1	chr19:56637133-56637661	K562	blood:	n/a	n/a
43	TBP	chr19:56637107-56637596	K562	blood:	n/a	n/a
44	CBX3	chr19:56637139-56637679	K562	blood:	n/a	n/a
45	NR2F2	chr19:56636942-56637690	K562	blood:	n/a	n/a
46	GABPA	chr19:56637113-56637514	K562	blood:	n/a	n/a
47	HMGN3	chr19:56637217-56637577	K562	blood:	n/a	n/a
48	ARID3A	chr19:56637231-56637617	K562	blood:	n/a	n/a
49	GATA2	chr19:56637171-56637633	K562	blood:	n/a	n/a
50	POLR2A	chr19:56637240-56637556	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56636040..56638265-chr19:56651210..56653201,2	K562	blood:
2	chr19:56637204..56640116-chr19:56644041..56647745,4	K562	blood:
3	chr19:56635952..56638231-chr19:56646331..56649019,3	MCF-7	breast:
4	chr19:56634814..56637617-chr19:56650729..56653163,3	MCF-7	breast:
5	chr19:56630485..56634048-chr19:56635782..56640573,5	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF787	TF binding region
ENSG00000142409	Chromatin interaction
ENSG00000167685	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs11673628	0.84[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs12459102	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12981138	0.84[ASN][1000 genomes]
rs12983086	0.89[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs2450439	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2631625	0.95[ASN][1000 genomes]
rs2631627	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2631628	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2631631	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2631637	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2631640	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2637088	0.86[ASN][1000 genomes]
rs2637092	0.94[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2637094	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2637097	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2637114	0.94[ASN][1000 genomes]
rs2932757	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs473953	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs478402	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4801676	0.84[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs481936	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs490345	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs492078	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs497453	0.95[ASN][1000 genomes]
rs501798	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs504350	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs506547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs509897	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs517021	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs517582	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs521092	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs522980	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs524778	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs524829	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs524988	0.95[ASN][1000 genomes]
rs525827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs527715	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs530102	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs533640	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs533734	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs535393	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs536342	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs536414	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs537425	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs540900	1.00[CEU][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.90[MEX][hapmap]
rs544365	0.88[ASN][1000 genomes]
rs545570	0.87[ASN][1000 genomes]
rs547002	0.86[ASN][1000 genomes]
rs547945	1.00[CEU][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs564050	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs564973	0.89[ASN][1000 genomes]
rs565879	0.82[ASN][1000 genomes]
rs569310	0.92[ASN][1000 genomes]
rs572851	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs578990	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs578991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs582271	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs583330	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs587702	0.86[ASN][1000 genomes]
rs588574	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs592827	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs599405	1.00[CEU][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.80[MEX][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs609736	0.97[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap]
rs619934	0.83[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs626821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs628090	0.88[ASN][1000 genomes]
rs629544	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs630704	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs640654	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs643133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs643174	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs648352	0.84[AMR][1000 genomes]
rs662308	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs662763	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs665082	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs665846	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs665857	0.94[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs667438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs667523	0.91[ASN][1000 genomes]
rs667974	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs669866	0.94[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.88[ASN][1000 genomes]
rs677127	0.94[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs677142	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs678540	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs684653	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs685117	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.90[JPT][hapmap];0.86[MEX][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8103672	0.84[CHB][hapmap];0.86[CHD][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs9676765	0.90[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
5	nsv833883	chr19:56512601-56640089	Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
9	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
11	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
12	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56633600-56637600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr19:56633600-56638400	Weak transcription	Spleen	Spleen
3	chr19:56633600-56638800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:56633600-56639400	Enhancers	Primary T cells from cord blood	blood
5	chr19:56633800-56637800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr19:56633800-56637800	Weak transcription	Fetal Kidney	kidney
7	chr19:56634000-56640800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr19:56634000-56645400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr19:56634400-56638400	Enhancers	Fetal Thymus	thymus
10	chr19:56636200-56639200	Enhancers	Fetal Muscle Trunk	muscle
11	chr19:56636200-56639200	Enhancers	Fetal Muscle Leg	muscle
12	chr19:56636800-56637800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:56636800-56637800	Enhancers	Fetal Stomach	stomach
14	chr19:56636800-56637800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr19:56636800-56637800	Flanking Active TSS	HepG2	liver
16	chr19:56636800-56638400	Enhancers	Placenta	Placenta
17	chr19:56636800-56638600	Enhancers	Pancreas	Pancrea
18	chr19:56636800-56639000	Enhancers	Colonic Mucosa	Colon
19	chr19:56637000-56637800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:56637000-56637800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:56637000-56637800	Flanking Active TSS	HSMM	muscle
22	chr19:56637000-56637800	Flanking Active TSS	K562	blood
23	chr19:56637000-56639200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr19:56637200-56637800	Enhancers	Fetal Intestine Small	intestine
25	chr19:56637200-56637800	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr19:56637200-56637800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr19:56637400-56637600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr19:56637400-56637600	Flanking Active TSS	Fetal Lung	lung
29	chr19:56637400-56637800	Enhancers	Fetal Intestine Large	intestine
30	chr19:56637400-56637800	Flanking Active TSS	HSMMtube	muscle
31	chr19:56637400-56645400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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