Tag | Content |
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EnhancerAtlas ID | HS180-01414 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:42363600-42364480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:42364220-42364235 | AGGTCAGCCTGCCCA | + | 6.23 | FOXP1 | MA0481.2 | chr1:42364236-42364248 | ATGTAAACAGAT | + | 6.62 | FOXP2 | MA0593.1 | chr1:42364236-42364247 | ATGTAAACAGA | + | 6.02 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_12188 | chr1:42362906-42366411 | CD3 | SE_20465 | chr1:42359593-42366379 | CD56 | SE_22944 | chr1:42362521-42366446 | CD8_primiary | SE_25331 | chr1:42362394-42369693 | DND41 | SE_31241 | chr1:42363139-42365158 | Fetal_Thymus | SE_39407 | chr1:42362477-42364743 | Jurkat | SE_44017 | chr1:42363252-42365108 | MM1S | SE_49913 | chr1:42362450-42365100 | RPMI-8402 | SE_66323 | chr1:42362477-42364743 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I041894 | chr1 | 42359742 | 42369334 |
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Enhancer Sequence | AGAGAGAGGG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGGTGCTGGG 60 AGAAGGAGGA CCCAGGGTGG AGGGAAAGGG CAGACCAGAG CCTCAGAGCC TGCCATCCCC 120 ACTGGCATCA TTTTGCTCTC ACAGGGCCCC TGCACTCTGC ACAATAAAGG AGTTGTTTAA 180 CCTCCCAGCA TCCTGGGGGC AGGAAATATT GGTTTCATCT ATTTGTTGTT TGTTTCAGTC 240 TTGGTGCATC TTGGAACCAA AGTTCTCACT GTATGGACAC AAAACTAATT TAGGTTCTTT 300 TAATCCAACA TAAGAAAAAC TTAGTTTCCT CTAGCCACCA TCAATCAACA CAAAGCCAAC 360 AGGGCGGAAG GGAGGGCCCT TGCTTCCTGG CAGTCTCCCT GGAGGGGGAG GGGGCAGGAA 420 GTGATCTAGA ATCCAGTCTC AGAAGAACTG CTGACAACAC CCTCACCAAA ACGCATCATC 480 ATCTTGCACT CATCTCTAAG TAGTGCCTCC CACAGCCTAA GAGCAAAGGC TCATAACTTC 540 TATCCACAGG GTTTCTGCCA TTTACCATTA CCTCCCTGTC CTGGCTCAGG CAAGGACCCT 600 CAGGGCTGAG ATGCATCTTC AGGTCAGCCT GCCCACATGT AAACAGATGA TACATGCACA 660 CGTGCGTGCA CACACACCCA CCTCTGCATG CTGGAGATAC ACAGGACGTG GAATAAGTCC 720 TCTCTGAGAA TTTACGAAGG CACCTGGCTG CCATCAGCAC AGAGTCATCC TCTGTCTGAG 780 TTCTGAAGGT AGCAGTGTCT CTGCAGGTAG GAAGAGAGAC AAATGGAGCT TCCTTCCAGC 840 TGAAGCAAGT AGAGGCTTTG TTTTCTCTCT AGAGGGTTGT 880
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