Variant report

Variant	rs11982656
Chromosome Location	chr7:100025812-100025813
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	MYC	chr7:100025735-100027621	Hela-S3	cervix:	n/a	chr7:100027575-100027585 chr7:100026944-100026953
2	E2F6	chr7:100025267-100027710	H1-hESC	embryonic stem cell:	n/a	chr7:100025863-100025870 chr7:100026011-100026025 chr7:100025863-100025870 chr7:100027410-100027419 chr7:100025861-100025872 chr7:100025862-100025871 chr7:100025941-100025950 chr7:100027323-100027332 chr7:100026924-100026933 chr7:100025862-100025870 chr7:100025862-100025874 chr7:100025863-100025870
3	RFX5	chr7:100025765-100027591	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr7:100025751-100028631	GM12892	blood:	n/a	n/a
5	YY1	chr7:100025734-100026568	HepG2	liver:	n/a	chr7:100026063-100026072 chr7:100026064-100026078 chr7:100025990-100026000 chr7:100025991-100025999 chr7:100026063-100026077 chr7:100026069-100026078 chr7:100026067-100026078
6	PAX5	chr7:100025547-100028145	GM12878	blood:	n/a	chr7:100027410-100027419 chr7:100027366-100027375
7	PML	chr7:100025656-100027778	MCF-7	breast:	n/a	n/a
8	POLR2A	chr7:100025653-100032091	GM12878	blood:	n/a	n/a
9	SP4	chr7:100025612-100027744	H1-hESC	embryonic stem cell:	n/a	chr7:100026919-100026935 chr7:100026492-100026503 chr7:100026838-100026854
10	NRF1	chr7:100025743-100028096	GM12878	blood:	n/a	chr7:100027409-100027420 chr7:100026982-100026993 chr7:100027319-100027333 chr7:100025940-100025954 chr7:100027322-100027331 chr7:100025940-100025951 chr7:100027322-100027336 chr7:100025940-100025951 chr7:100027409-100027423 chr7:100027322-100027333 chr7:100026924-100026933 chr7:100025940-100025949 chr7:100025942-100025951
11	GABPA	chr7:100025566-100028962	K562	blood:	n/a	chr7:100027409-100027420 chr7:100027319-100027333 chr7:100025940-100025954 chr7:100027322-100027331 chr7:100027322-100027336 chr7:100025940-100025951 chr7:100027409-100027423 chr7:100027322-100027333 chr7:100026924-100026933 chr7:100025940-100025949 chr7:100025942-100025951
12	GABPA	chr7:100025468-100027226	SK-N-SH	brain:	n/a	chr7:100025940-100025954 chr7:100025940-100025951 chr7:100026924-100026933 chr7:100025940-100025949 chr7:100025942-100025951
13	POLR2A	chr7:100025752-100027995	HepG2	liver:	n/a	n/a
14	NR2F2	chr7:100025392-100028801	K562	blood:	n/a	n/a
15	BHLHE40	chr7:100025725-100028316	GM12878	blood:	n/a	chr7:100026063-100026079
16	ATF3	chr7:100025721-100027216	A549	lung:	n/a	chr7:100026893-100026906 chr7:100026924-100026933
17	SP4	chr7:100025566-100027287	H1-hESC	embryonic stem cell:	n/a	chr7:100026919-100026935 chr7:100026492-100026503 chr7:100026838-100026854
18	POLR2A	chr7:100025689-100027930	PBDE	blood:	n/a	n/a
19	RCOR1	chr7:100025682-100028267	GM12878	blood:	n/a	n/a
20	TAF1	chr7:100025693-100028086	SK-N-SH	brain:	n/a	n/a
21	ZNF143	chr7:100025729-100027563	Hela-S3	cervix:	n/a	chr7:100026022-100026040 chr7:100026024-100026033 chr7:100026022-100026031
22	TAF1	chr7:100025669-100027873	H1-neurons	neurons:	n/a	n/a
23	GTF2F1	chr7:100025702-100027275	Hela-S3	cervix:	n/a	n/a
24	KAP1	chr7:100025622-100026963	U2OS	brain:	n/a	n/a
25	CREB1	chr7:100025672-100026577	A549	lung:	n/a	n/a
26	POLR2A	chr7:100025745-100027965	HepG2	liver:	n/a	n/a
27	TEAD4	chr7:100025675-100026143	H1-hESC	embryonic stem cell:	n/a	n/a
28	ELF1	chr7:100025584-100027755	MCF-7	breast:	n/a	chr7:100026064-100026076
29	GABPA	chr7:100025594-100026347	A549	lung:	n/a	chr7:100025940-100025954 chr7:100025940-100025951 chr7:100025940-100025949 chr7:100025942-100025951
30	EGR1	chr7:100025723-100027445	K562	blood:	n/a	chr7:100027323-100027332 chr7:100026021-100026045 chr7:100026923-100026933 chr7:100027410-100027419 chr7:100026924-100026934 chr7:100025941-100025950 chr7:100027010-100027024 chr7:100027229-100027242 chr7:100026454-100026468
31	RCOR1	chr7:100025702-100027606	K562	blood:	n/a	n/a
32	SIX5	chr7:100025803-100026277	H1-hESC	embryonic stem cell:	n/a	chr7:100026024-100026033 chr7:100026041-100026057 chr7:100026020-100026034 chr7:100026022-100026031 chr7:100026019-100026028
33	THAP1	chr7:100025742-100026073	K562	blood:	n/a	n/a
34	MYC	chr7:100025681-100028419	K562	blood:	n/a	chr7:100027575-100027585 chr7:100026944-100026953
35	CTCF	chr7:100025800-100025950	HMEC	breast:	n/a	chr7:100025909-100025922
36	USF1	chr7:100025758-100026088	A549	lung:	n/a	chr7:100026063-100026079
37	RCOR1	chr7:100025435-100027542	K562	blood:	n/a	n/a
38	MYC	chr7:100025742-100026323	H1-hESC	embryonic stem cell:	n/a	n/a
39	ELK1	chr7:100025761-100027165	GM12878	blood:	n/a	n/a
40	MAX	chr7:100025321-100028257	HCT-116	colon:	n/a	chr7:100027575-100027585 chr7:100026944-100026953
41	POLR2A	chr7:100025780-100027981	H1-hESC	embryonic stem cell:	n/a	n/a
42	TAF1	chr7:100025796-100027986	H1-hESC	embryonic stem cell:	n/a	n/a
43	IRF1	chr7:100025736-100028321	K562	blood:	n/a	chr7:100026838-100026852 chr7:100026923-100026937 chr7:100025758-100025769 chr7:100025806-100025820 chr7:100026818-100026832
44	CREB1	chr7:100025648-100027823	HepG2	liver:	n/a	n/a
45	POLR2A	chr7:100025635-100029589	Hela-S3	cervix:	n/a	n/a
46	CEBPD	chr7:100025553-100028942	K562	blood:	n/a	n/a
47	GABPA	chr7:100025503-100027620	MCF-7	breast:	n/a	chr7:100027409-100027420 chr7:100027319-100027333 chr7:100025940-100025954 chr7:100027322-100027331 chr7:100027322-100027336 chr7:100025940-100025951 chr7:100027409-100027423 chr7:100027322-100027333 chr7:100026924-100026933 chr7:100025940-100025949 chr7:100025942-100025951
48	POLR2A	chr7:100025801-100028460	IMR90	lung:	n/a	n/a
49	MAX	chr7:100025597-100028390	NB4	blood:	n/a	chr7:100027575-100027585 chr7:100026944-100026953
50	MXI1	chr7:100025736-100027954	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100024810..100029555-chr7:100269638..100276218,15	K562	blood:
2	chr7:100025040..100027512-chr7:100201980..100203554,3	K562	blood:
3	chr7:100024854..100029212-chr7:100238393..100241596,5	K562	blood:
4	chr7:100025071..100027924-chr7:100727777..100730095,3	K562	blood:
5	chr7:100024700..100032514-chr7:100067180..100083143,31	K562	blood:
6	chr7:100024644..100031194-chr7:100062394..100068680,9	K562	blood:
7	chr7:99677060..99680949-chr7:100024846..100027547,5	MCF-7	breast:
8	chr1:6295787..6296432-chr7:100025799..100026713,2	NB4	blood:
9	chr7:99743864..99749368-chr7:100025322..100029105,6	K562	blood:
10	chr7:100025569..100027511-chr7:100253508..100255447,2	K562	blood:
11	chr1:145382627..145383409-chr7:100025751..100026749,3	Hela-S3	cervix:
12	chr7:99677846..99681399-chr7:100025174..100029012,4	K562	blood:
13	chr7:100025231..100027840-chr7:100303669..100306614,3	K562	blood:
14	chr4:164413226..164415880-chr7:100024994..100026878,2	MCF-7	breast:
15	chr7:99753605..99756389-chr7:100024404..100026585,2	MCF-7	breast:
16	chr7:99715745..99719819-chr7:100025787..100030155,6	K562	blood:
17	chr7:100025375..100027426-chr7:100270912..100272757,2	K562	blood:
18	chr7:99695452..99699124-chr7:100025277..100027831,3	MCF-7	breast:
19	chr7:100014519..100016131-chr7:100025765..100027898,2	MCF-7	breast:
20	chr2:183580551..183581074-chr7:100025798..100026773,2	Hela-S3	cervix:
21	chr7:99697437..99703178-chr7:100024624..100029482,10	K562	blood:
22	chr7:100025223..100026949-chr7:104653159..104655060,2	MCF-7	breast:
23	chr7:100009272..100011233-chr7:100024353..100026026,2	MCF-7	breast:
24	chr1:11967024..11970880-chr7:100024808..100027879,3	K562	blood:
25	chr7:100024823..100028490-chr7:100199635..100204792,9	MCF-7	breast:
26	chr11:67273139..67273801-chr7:100025739..100026564,2	Hela-S3	cervix:
27	chr7:100004091..100007847-chr7:100024893..100029911,8	MCF-7	breast:
28	chr7:99744731..99747065-chr7:100025501..100027244,2	MCF-7	breast:
29	chr7:100024866..100028113-chr7:100485356..100489963,5	MCF-7	breast:
30	chr7:99696789..99700792-chr7:100024893..100031468,10	K562	blood:
31	chr7:100024969..100026513-chr7:100273974..100276218,2	MCF-7	breast:
32	chr7:100009832..100015861-chr7:100024427..100028524,9	MCF-7	breast:
33	chr7:99965641..99971124-chr7:100025245..100028820,5	MCF-7	breast:
34	chr7:100025163..100029050-chr7:100284721..100290800,5	MCF-7	breast:
35	chr7:100024988..100028445-chr7:100180808..100186978,10	K562	blood:
36	chr7:100024682..100026645-chr7:100273094..100274953,2	K562	blood:
37	chr7:100025040..100027312-chr7:100198003..100200781,2	K562	blood:
38	chr14:90863251..90863952-chr7:100025800..100026571,2	HCT-116	colon:
39	chr7:99939167..99940736-chr7:100025324..100028004,2	K562	blood:
40	chr7:99998688..100005691-chr7:100025198..100032529,13	K562	blood:
41	chr7:100024981..100028086-chr7:100074705..100078040,4	MCF-7	breast:
42	chr7:100023646..100028399-chr7:100166149..100169452,5	K562	blood:
43	chr20:47662860..47663424-chr7:100025812..100026750,2	NB4	blood:
44	chr7:100025394..100027753-chr7:100083399..100085639,3	MCF-7	breast:
45	chr7:100025648..100028089-chr7:100060408..100062284,2	K562	blood:
46	chr2:122288253..122289239-chr7:100025777..100026902,3	Hela-S3	cervix:
47	chr7:100025040..100028858-chr7:100198464..100203953,10	K562	blood:
48	chr7:100025028..100029218-chr7:100206824..100213289,7	K562	blood:
49	chr17:26971940..26972827-chr7:100025757..100026809,3	HCT-116	colon:
50	chr11:82996396..82997341-chr7:100025735..100026579,2	Hela-S3	cervix:

Variant related genes	Relation type
MEPCE	TF binding region
ENSG00000146833	Chromatin interaction
ENSG00000007202	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000085514	Chromatin interaction
ENSG00000121716	Chromatin interaction
ENSG00000087087	Chromatin interaction
ENSG00000184414	Chromatin interaction
ENSG00000255234	Chromatin interaction
ENSG00000074054	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000266372	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000160917	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000242798	Chromatin interaction
ENSG00000166997	Chromatin interaction
ENSG00000077232	Chromatin interaction
ENSG00000091986	Chromatin interaction
ENSG00000266154	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000221838	Chromatin interaction
ENSG00000185955	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000106333	Chromatin interaction
ENSG00000201801	Chromatin interaction
ENSG00000004975	Chromatin interaction
ENSG00000137500	Chromatin interaction
ENSG00000213420	Chromatin interaction
ENSG00000225077	Chromatin interaction
ENSG00000106290	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000146826	Chromatin interaction
ENSG00000222724	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000166526	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000066923	Chromatin interaction
ENSG00000224729	Chromatin interaction
ENSG00000124207	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000106246	Chromatin interaction
ENSG00000239569	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000198498	Chromatin interaction
ENSG00000198668	Chromatin interaction
ENSG00000116237	Chromatin interaction
ENSG00000214309	Chromatin interaction
ENSG00000106327	Chromatin interaction
ENSG00000264229	Chromatin interaction
ENSG00000078319	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000106330	Chromatin interaction
ENSG00000077080	Chromatin interaction
ENSG00000087077	Chromatin interaction
ENSG00000264758	Chromatin interaction
ENSG00000188186	Chromatin interaction
ENSG00000106351	Chromatin interaction
ENSG00000169871	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs11975190	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv527107	chr7:100014711-100064719	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	269 gene(s)	inside rSNPs	diseases
5	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
6	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
8	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
9	esv3329388	chr7:100023441-100025989	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
10	esv3330521	chr7:100023666-100025889	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	72 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99995000-100026000	Weak transcription	Primary T cells from cord blood	blood
2	chr7:100011600-100026000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:100025200-100026000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:100025400-100026000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
5	chr7:100025400-100026000	Enhancers	Primary B cells from cord blood	blood
6	chr7:100025400-100026000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:100025400-100026000	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr7:100025400-100026000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr7:100025400-100026000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr7:100025400-100026000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:100025400-100026000	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr7:100025400-100026000	Flanking Active TSS	Colon Smooth Muscle	Colon
13	chr7:100025400-100026000	Flanking Active TSS	Placenta	Placenta
14	chr7:100025400-100026000	Enhancers	Fetal Thymus	thymus
15	chr7:100025400-100026000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr7:100025400-100026000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr7:100025400-100026000	Flanking Active TSS	Dnd41	blood
18	chr7:100025400-100026000	Flanking Active TSS	HSMMtube	muscle
19	chr7:100025400-100026000	Flanking Active TSS	Osteobl	bone
20	chr7:100025400-100026200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:100025400-100026200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr7:100025400-100026800	Flanking Active TSS	Stomach Smooth Muscle	stomach
23	chr7:100025400-100028200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:100025400-100028200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:100025400-100028200	Active TSS	Brain Germinal Matrix	brain
26	chr7:100025400-100028200	Active TSS	Fetal Brain Female	brain
27	chr7:100025400-100028200	Active TSS	Rectal Smooth Muscle	rectum
28	chr7:100025400-100028600	Active TSS	Fetal Kidney	kidney
29	chr7:100025400-100028800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:100025600-100026000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:100025600-100026000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:100025600-100026000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
33	chr7:100025600-100026000	Flanking Active TSS	Primary B cells from peripheral blood	blood
34	chr7:100025600-100026000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr7:100025600-100026000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:100025600-100026000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr7:100025600-100026000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr7:100025600-100026000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:100025600-100026000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:100025600-100026000	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr7:100025600-100026000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr7:100025600-100026000	Flanking Active TSS	Fetal Brain Male	brain
43	chr7:100025600-100026000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
44	chr7:100025600-100026000	Flanking Active TSS	Fetal Lung	lung
45	chr7:100025600-100026000	Flanking Active TSS	Fetal Muscle Trunk	muscle
46	chr7:100025600-100026000	Flanking Active TSS	Fetal Muscle Leg	muscle
47	chr7:100025600-100026000	Flanking Active TSS	Lung	lung
48	chr7:100025600-100026000	Flanking Active TSS	Pancreas	Pancrea
49	chr7:100025600-100026000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
50	chr7:100025600-100026000	Enhancers	Sigmoid Colon	Sigmoid Colon

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