| Tag | Content |
|---|
EnhancerAtlas ID | HS180-48955 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr9:38380530-38381900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr9:38380620-38380630 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr9:38380619-38380630 | TTTCACACCTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_01762 | chr9:38380680-38383801 | Aorta | | SE_28948 | chr9:38378684-38384162 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 38380679 | 38381519 | | chr9 | 38381534 | 38381667 | | chr9 | 38381693 | 38381840 |
|
Enhancer Sequence | AGTGCCTCCT GCTATATCCC CTCTTATGAA TAGAAAGATT CAGTAGATCA CTTACTCAGT 60
GACCTTTTCA GGTGCACTAA AACCAAGCAT TTCACACCTT AGGGAGACAC AAGGCAGGAT 120
CTAATCAGAA CTCTGCATCC CTCGGGCTTG GTTTAGGGAT TCTAGTGCCA CATTCAAAGC 180
ACAGAACAGG CGCCTGGGCC AATGTCACCT TGGTAAGTGT CTGCCTCCCA GCGTGCCTTA 240
AGGTTGCAGG AAATTGCCTA TTTACACGTA TTCTGCTCTG ACAGGCACAC CAGAATTTTA 300
AAATCCTCCT TCAGGTTTCT CACAGATAAG ATGGGGAACT TTGTTTACTA TGGATTCCAG 360
GGCTTCCTGA AGAGGAGGCC TTTGAGTTTT CGAAAATAAT TGCTTTTCCT CTCCTGTGCT 420
CTCCAGGGGT GGTCTTTGGC CGGAGGAAGA AATGGCTTTG TTGCTCAGGA GAGCTTTGGG 480
AATGGAACTC AGGGGCTTCC AAAGAGCAGC AATCAGGAAA ACAAGCAGGG AGGATCCAGG 540
TTTTGCAAGG CCTGAAGCCT GCACACTAGG GAGCCCCATG CTCTGTGAAG GAGAGAACAG 600
TGATAAGAAG AAGATAATGA TTCAGCAGCT TTGCAAACAT TGTTTGGTGA ATAAACAGCC 660
CCGTTCAGTG CACCGGTTTC TTCCTCCCAT CATGGGACAG GTGGAATGTG ATCTGAGATG 720
CCAGCCTTGG TCAGCTGGAG GGTTGTTCAG CTGCCTCGTG ACTCCTCCTC GGTAAGAGTG 780
AAAGAGCCTT TCATTCCCTA AATAAACATG TCTATTAGAG GCATTGATCT GTCCCCAGCA 840
GGCAGTAATT GCACCTCAAA TGCCACAGAT GCACAGCCTG GGGTTCTACT CCACCCCGCC 900
CTGCCCTGCC CTGCCAGTCT CCCTGCCTGG CCTGGGACGG ACCCTGACCC TCCTTGGGGT 960
TCAGGCTCTT CTTCTGTACA GAGTCACAAG GCTGTTAATT CATATTCTTC CCATCACAGG 1020
GATGAACCCC TCTGGCTCAG TCATAAATGA TAATATAAGA CTCGTTTTCC ATGGAAAAGC 1080
CCTAGTACAG CCATACGGGT ACTTTAATAC AAAATGCTCA CCTACCAGTT TGTAAGCAGC 1140
CCCTCTCTGA GCCCCTAGGT GCCACCTCCA CTCTGTCCTC ACGGCCCTTG GCCTGGGACC 1200
CCCTGAACTT CCGCATGACT CACCATGGCC AACCAGATCA CAAGGGTTAG GGTTAGGGTG 1260
AGCACAGAAT TACAGCCAGG CTTTGTGCCC ATGCTCCATT CCTCAGTATA TCAAATCTCA 1320
CCCCTGGGCC TGGGCTGGGG CCCCTGCACA GGCTCCAGCC CTTCTTAGCC 1370
|
