| Tag | Content |
|---|
EnhancerAtlas ID | HS180-09656 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:94885920-94887340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr11:94885951-94885963 | GATTGTTTTTTT | + | 6.44 | | IRF1 | MA0050.2 | chr11:94886462-94886483 | GTAATGAAAGTGAAACTGCGT | - | 7 | | IRF8 | MA0652.1 | chr11:94886465-94886479 | ATGAAAGTGAAACT | + | 6.06 | | IRF9 | MA0653.1 | chr11:94886464-94886479 | AATGAAAGTGAAACT | + | 6.38 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36837 | chr11:94885982-94887101 | HMEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGATTTACA TATATATAAG ATTTTCTGTC TGATTGTTTT TTTGGGTATG AGAAAAAGAC 60
AGGAATCAGG GATGACTCCA AGCAGCTGGA AAAACGGAGA TGCTGCTGGC TGAGATTGGA 120
AGATGCTGGG GTAGAGGGAT AAGACAGCTT AATGTTATAT ATTTTAGGTT TGAGGTGTTC 180
ATTAGAAAAA CAAGTGGAGA GATTGATTGG GCAGACACAC AGGTCTGGAG AGGGCTGGGC 240
TGGAGATAGA AATATGGGTT GCCATGATAC AGGCATGGGA CTGAAAGCCC CATCAGTCCC 300
TTGGAGAGAT CATCAGAGAG TGAGTAGAGA CATAGCAGGG CGAAGCCCTG AGCCCCGGTT 360
CCCCCAGCAT GTACCTGCAG TCTGTTTCCT CTTCTCAACT ACAATTCCCA TGGTCTTGTC 420
TTGTTCACAG AACCTGCTCA AGGAGCATCT ATTAAATGAA GGAACCCAAC TTTCATCACA 480
TGTAAAATAA ACATCATTAT AATCCTACCT CATAAGGTTG TTGTCAGAAA AAGTTAAACG 540
TCGTAATGAA AGTGAAACTG CGTTATGATT GGTAGATGCC TGCTATATTT TAAAATGTAG 600
GCTTCATTAT CTCATTCTGT ACAGCTTGTA TTACTTGATT GTATCTTCAC AGTTTCTGAT 660
GCATGCAAGG CAGACACTCT CGTTCTCACT TTATTGACGA GGAAAGTAGG ATTGGTGAGA 720
CAAAATAAGT CCCTGAAGCT GCATATCTAA TGGTAACACC AGTGGCTGAC CTGTTTGAGC 780
ACATCTGCGG CAGGCACTGT GTTAATGATT TTGCATGTGT TATCTGGCAA CAACACAGCG 840
AGGTGGGGGT TATTATCTTC ACTTGCACAT GAGGAAACTG AAGCATAGAG AGGGTGGTTA 900
ACTTAGCCAA GGTCCCATAG TGAGTGGTTG GAAGAGTCTG GGCCATGAAG CAGACCTGCC 960
CATCCTGATT CAATGTTCTT TTTGCAGCCT GATAGCTCCT CTTCTTCATC CCCCTACTAG 1020
ACTCCTGCCA GGGCCAAGCC TCACCACTCC TTCCCTTGAC ATTGGCAACA TTCCTCTCTC 1080
CTTAACGTTT CTCTCCTACC AAGCCTGCTT GCTGCAGGAT ACAAGAGTTC AGTCACTCCT 1140
TGGGAACAAC CTGCAGGTCA AAACATTTTG GCTTATTGCT TCCCCTTTCT GGAAAGTCCT 1200
TTCCCTTCCT CTCTGCCTTA TGAACTCCTA TGTGTTCTTC CAAACCCTGG TGAACTCCTA 1260
TGTGGTTTTC CAAGTCCAAT TAATATGTCA CCTCTGTTGT GAAGCTTTCC CTGCTTGCAC 1320
CAGACAAGAG GCATGACTTA GATCATGTGA CACTTTGTTT ATAGGTCTAT CAAAACAAAC 1380
TGACAATTTC CTGTGGGTTT GACTGATGCC CCTGTAATAT 1420
|
