Tag | Content |
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EnhancerAtlas ID | HS104-37862 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr21:39037250-39038640 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr21:39038424-39038435 | AAACCACAGAA | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 39037573 | 39037642 | chr21 | 39037875 | 39038167 |
| | Number: 1 | ID | Chromosome | Start | End |
GH21I037665 | chr21 | 39037324 | 39038271 |
| Enhancer Sequence | CCGCGCCCGG CTAATTTTTT GTATTTTTTA GTAGAGACGG GGTTTCACCG TGTTAGCCAG 60 GATGGTCTCG ATCTCCTGAC CTTGGGATCC GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT 120 TACAGACATG AGCCACCACG CCTGGCAAGA ATATTCCTTT TAAGCCTTGG TTTAGTCATT 180 TGCCAAATGG GTCAACAATG GCACAAATCT CACTGGATCC CTGTGAAGAT TAAAGCAGAT 240 AATGAATAGA AGTATCTTGC AGCAAGCAAG AGAAAGGTTC ACTGGCACAT AGGATGCATT 300 AAATAAACAG TAACTATTAT TATCATTATT TATGATTATT GATGGTTCCC AAGAGAGCCT 360 CCCTGGCAAG GCAGGCCATG GTGCCAGTCG TCTGTATAAG TCCATGCGAT CATTGAAAGC 420 ATTATTTCTC CAGGAATGAG GTAGTCATTG TTCTCTGGTT TTACAATATA CATTTAGCAA 480 TTGGCAGGAT GTGGACGAAC CTCATGGGAA TCGGAAGTAG CTCTGAATTG TAAAGAGAAA 540 CAGCCAGATC AGATAGGAAA GTAATTTTTA ATTACTCCGC TGAATTTCTA GCAGGGAGAT 600 TGCAACCTTG GTGAGTGAGT CTCCATGCTG GTATGAGGTA GAGCTGGATT TGGACAGCTC 660 AATGCAGGTG TGCCAACCTT TCCTTCCTCT CTCAGTGGAC AAGGAAGGGA GGAACAAGAC 720 TAAAATACAG TTTTAGGTCG ACCAAGTGTC TGCTCGCTGA CATCATTCAT CCCTCCCTCA 780 AGTATCACAG ACAATTTTTG TAGCCGAGCG TTGCTGCTGT TTAGTAATTC AAAGTGTATC 840 TGAGAAACAC AATTATCTCG ACAGAGAGTT GGACAGCAGC TGAGGGTGAT GTGTGAGCTG 900 GTGCCAGAGG TTTGCTTGTT TAGTTACTCC AAGCAGGGAG TTGTCATAAG GCTTCCTGGA 960 GGAGTGGAGC TGGGGGCAGA GAGTGGCCTC TCACTGGATG CAGGTAGAAA AAGGAGCCAG 1020 AAATGAGCAG GCCCAGCTAG TTGCTGGATT GGCTAGTTGC TACCATGATG TCATTTCATA 1080 CCCACAGCCA CCCTGAAACC TGAAAGCAAG GTTTTATCAC TTCCCATGTT GCAGGTTAGA 1140 AGACATGGCT TGCACAGGTG GAGTGATCCT TCCCAAACCA CAGAAGCGGG AGTGAAGGGA 1200 TCCTATCCTT GGGCAGAGGC TCAGAGGGGA GAAGATGGGT ACACAGGCAG AGATCTGGGA 1260 ATGGCAAGGT CAGCTTCTAG TGGCCCAAGA ACCCCTAGTT CTGGCTTCCT GTTGAGTAGG 1320 ACCAAGTCCT CACTCCCCTT CCCCTGGGAT TCCTCAGGCT GACCTGAGGC TGAGCTGACT 1380 CTCACGGTTT 1390
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