| Tag | Content |
|---|
EnhancerAtlas ID | HS112-10243 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr3:141514060-141515720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr3:141515245-141515256 | AGGCACTCAAG | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 141514066 | 141514497 | | chr3 | 141515444 | 141515577 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I141795 | chr3 | 141514089 | 141518069 |
| Enhancer Sequence | GGCGGGTGAT TGTGCCAAAC TTCCTGGGGA TACTTGGCAA TGTCTGGAGA CAGTTTTGGT 60
TGTCATGACT GGGGAACTGC TACCAGCATC TAGTGGGTAG AGGCAGGGAT ACTGCCAAAC 120
ATCTTACAAT GAATAGCACA GCCCCCAACA CAAAGCATAT TCAGCCCACA ACATCCACAG 180
TGCCACACTT GAAAACCCTG GCATAAAGGC CTCGCAGCAC AAGGCCTGAG GCTCAGTCGC 240
AGAACAGAGT GGCTTTGCAG CTGGCTGCAG TGTGGAGTCA TGAGGTGGGA GGGGTGACTA 300
ACGATACAAC TAGAGAGTTT AGCAGACACC AGGCCCTAGG GGCTGGAGGA GTTGCACAAG 360
GGGAGTTTGA ACCTATTGGC AAGGGTGCTG GGGAACCGAT GAAAGGTTTT TAGCAGGGAA 420
GTGACAAAAT CAATCTTGGG GCCAGGTGTG GTGGCTAATG CCTGTAATCT CAGCATTTTG 480
GGAGGCCAAG GCACAAGGAT TACTTGAGCC TAGCAGATGG AGACCAGCCT GGGCAACAAA 540
GCGAGACTCT GCTCTATGTT AAAAAAAAAA AATAGCCTTG GAATTACATC AAAGAGAAGG 600
AGTTAGAATG AGCACAGAAA GGCTGGGAGG GAAGCAGAGG ACTCAGGGAA CTGTGGGCTT 660
GCACATTGTC TAATGGAGTC ACGGGAATAA GGAGAGGCTG GGCCAGGGGG TCTGCAGGAT 720
GCGGCAGGAG GGGGCTGTCA TGTGACATGA TACAGTTCAG GGACCTAATG GTTGCCGTGT 780
CATCTAATCT AATATAGACA CATGTTAGAA GCTCAGAGCA TTCATTTAGA TCATGCGCAG 840
CTGATGAAAT ATAGTCCTGC AGGTCAAGGA GAAAGGAGCT TGAGCATTTG AATCCTGGTT 900
CTGCCACTTA CTCTGGCTGC TGTGTACAGA TGTGCAGGCT GACTCCCTGC ATGGGAGAGT 960
GGGGGCTGAC GTCACATGGG AGGCTGGTTT GCTCCACGCA CCAAGACATT TGGAGTGCCT 1020
TCTAATTGGC ACAAATGTAC TCATGGGTTG GCCACAGCCC TGCACATGAT CTTACACAAG 1080
TCAGACTGCT TCTCTGAGCC TGCTTAATAC TGCCTGCCTT TAGCGTTGAT GAGAAGATTA 1140
AGAAACAAAG TAGATAAATG CCTAGCCGAG GGTCAGCCAC TTGGTAGGCA CTCAAGAAAT 1200
GATTGTACAA GAAGCTCCAG ACCTTCAGTC ACAATCCCCG CTGTTGCAAT TGTTTCTGCC 1260
TCACCTGACA GGCACTGTAG TTGCTCAGGT GACCTCTGCA GCTGTGCTTT GTTCTCTGCG 1320
AGGCACAGGG AGCCAGCGGG ACCCCAAGGC TGCAGCAGTG GGCAGTGGGT GAGCAGCTTG 1380
CATCTGGGTT GAGCCAAGCA GACACTCACA GTTGTCTTGC TTCCTCACAG CTGTGTGGGG 1440
TTTCATTTGT GGTTTTCTTC TGAGCATCTT AGAGGCACCG TGGAAAGTAT GCCTCAGCCT 1500
GCTGCCAGAG AGATTCATAG CACATGAAAC CACTGAAGAA CACGCTCAAG TGAAAGAACG 1560
GGAACTATTG ATCTCTGACC ATGTGCCAGG CCCTGCCTTT CAGTCTGATG GAGTCTTGTG 1620
TAGCTGTCCT GCCTGAGACA ACCAGAACCC AGGCATGGTA 1660
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