Tag | Content |
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EnhancerAtlas ID | HS048-20567 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:69786450-69787460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Six3 | MA0631.1 | chr2:69786858-69786875 | CCATGTGATACCCTTTA | - | 6.4 |
| | 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 |
GH02I069559 | chr2 | 69786733 | 69787332 |
| Enhancer Sequence | AAAATGCATG TTTTTTACAT TTTGCTTTTT AGGGTATCAG AATGTCTTGT AATAAAAATG 60 TGCATTTAAT GCAGTGGTAT TTATCTTTTC TTCCCCCCAC CCCCTGCCAA AGTTATTAAA 120 TCCATGATGT TCTCTTATAA TTAATCAGAA TTGAGGAAAA TAGTAGTGTA AATTACAAAA 180 TTTCTATGTA TGTTCATAAT TGTTTTGTAA ATAGTATAAG TAGGATTCAC TTCATTGATA 240 TTTAGAATTT TTTAAAAAAT CACGGAACTA CAGACTTCAC AAGAGTGGCA CTCCTAGAGA 300 GTATTAAGTC CAAGTGTTTT GCTTTATGCA TAGACAAACC AAGAGAGGCT TAGGAGTCCC 360 ATGGCTAGTT ATGGGCAGAA GGTGGGGTGG TTCTCTCTCC TATAAAAACC ATGTGATACC 420 CTTTAGGTAA TAAGGAAACA GCTGACAATG TTGTGAAACA AAAGGTGGGA ATAGGTATTT 480 CCTACAGTTC AATGATGCCT GTCACTGCTG AAGGACAAGG CAACTCTTTC AGATGCTGCA 540 ATTTGAGATA ACTACCACCA GATGGGAGCA GTGTAGTTTT CTTTGTAGGT AGCAAGATGA 600 CCTTTACAGC CAGGACTGAA GAAATGGGTC AGTCGCCTAC CATGCAATCC AGTAAGCACA 660 ATGGCTGACA AGAGCCAGCC CAGATTCTCA AAGCCTATGA CCATGATAAA TCTAAAAGCA 720 AATCAGTGAA TCACTTTACT TAACACAGAT GAAGCCACAT TGTCAAGCAT CTATGCCTAT 780 AAAAGGGCTT ATCTGCAGAT GAGAAGCATT TAAATCACGA GATCAAAATC CACGCCTAAC 840 AGGACTTGTC AGTCTAAAGA TGTTGGTCAC TATCACTGTG TAGTTGGCCA AATGGAGATG 900 TAAACTAGGT TAGAAGAGAG GAGATAGTGC CATTCAAGAT ACTTCTCGTG CACAGCCCTG 960 TCTGTCACAC GGATCAGGGT GATGAGATTC TCAGCCAGAG CTTAAGAGGG 1010
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