Tag | Content |
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EnhancerAtlas ID | HS050-03285 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:92021250-92022380 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:92021946-92021961 | TGCTGAATCATGCTG | - | 6.9 | TBX20 | MA0689.1 | chr1:92021640-92021651 | TAGGTGTGAAG | + | 6.62 | TCF3 | MA0522.2 | chr1:92022220-92022230 | AGCAGGTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_12473 | chr1:92019276-92023330 | CD3 | SE_20281 | chr1:92010459-92026642 | CD56 | SE_22755 | chr1:92009684-92026666 | CD8_primiary | SE_44373 | chr1:92017171-92023273 | NHDF-Ad | SE_45456 | chr1:92020995-92021904 | NHLF | SE_45456 | chr1:92021997-92022623 | NHLF |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I091545 | chr1 | 92010992 | 92023982 |
|
Enhancer Sequence | AGTGTGTTTG TGAGGTCAAA TTTTTGCTTC TTAGAATAAG AGTCACTTTG ATTTTGGTGG 60 GGCAGGATCA CCCGTGGGAG GATAACTCAT CCACACATAT CAGACATGAA TCCTTCAGTG 120 AGAGATGGGG AGTGGGAGCA GAGTGGTCAG GGTATCCCTG TGAGGCAAGG GAGGGATCCT 180 GACCTCTGGT GCACCTGACC TCTGGGGGAC TGGCTCTTGG GTCCAACTCA AGGTTCCTTT 240 TCAGGGCCTG TGGCATGTCC TCCAGGCCAT ACTGCCATCT TTAAAATACT GCCGGCACCT 300 AGTTGTTACT GTCAGCACCT GGCTGTGGTA GGGGAGGACA GACACCGATG ATTCACGAGG 360 CGTGATCCAG AGCATTGTAA CCATTAGTAG TAGGTGTGAA GGGAAATCAT CAAACCATGT 420 GAAGGTGGGA AAAGTTGTCA CAAGTTGCAA ATCTATAAGA CAAAACTGTA AGACCAATGA 480 AAATATTGAA AAAATTCACT GCACTCTATG AGGCTGCTGT GAGAAGCAAA AGAAGCAAGT 540 GTAAAGCCTT CAGGTGTCAC AGAAATAGGC CCCTGATCGT GCCTCAAACC ATAAGACGTC 600 AGAGCATGAA ACACCAGTGA GGGAGAGTGA TTGCGTTTCA CAGATAAAGA GCCTATGAGC 660 AAAACCAATC TTCCTTTCCT CTGAAGTGTG CCCCATTGCT GAATCATGCT GATGAGTTAT 720 CATGGTTTTC CTCCTGCATG ATTTTCTTCT GTAATACTCA TTTCAGAAGT TAAAAAAAAA 780 ACAACAAAAC AAAACACAAC AAAAAAACCT GCTACCTGTT TCTCTTTTTA ATCCTGCATT 840 TTAACAGACA GGCCAAGAGC AGGAGCAATT AGTCTCCCTG AGGATTTGCA AAGGGGAATT 900 CCAATTGTGA GCGAGCTGTC ATCCTTCTCC TTCAGTTGTT TAAATGTGAT TCCATCTAAT 960 TCAGTTCCAG AGCAGGTGTT GAGCATCTTA TGTGTGCAGA CACTTACTAG GCACTGCTAG 1020 GATAGACTAG GACAGGCAGG ATGCTGCCAC TGCCCAGGTG GAGCACATCA TCAAGCGGGG 1080 GCCACAGAGA CATAGACAAA TAGTTATCTG GAATTACAAT GTGGAACAGA 1130
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