Tag | Content |
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EnhancerAtlas ID | HS034-22683 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr4:25564460-25565490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr4:25565068-25565079 | TAAGTAAATAT | + | 6.14 | FOXF2 | MA0030.1 | chr4:25564933-25564947 | TTTGTTTACCTTCA | - | 6.38 | Foxd3 | MA0041.1 | chr4:25565471-25565483 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr4:25565475-25565487 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr4:25564766-25564776 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr4:25564766-25564776 | GGCACGTGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCTGGAGTG CAGTGGTGCA GTGGCGCGAT CTCGGCTCAC TGCATCCTCC ACCTCCTGGG 60 TTCAAGTGAT TCTCCTGCCT CAGTCTCCTG AATAGCTGGG ATTACAGGCA TGCACCATCA 120 CACCCAGCTA ATTTTTGTAT TTTTAGTAGA GAGGGGTTTC ACCATGTTGG CCAGGCTGGT 180 CTCAAACTTC TGATCTCGTG ATTTGCCTGC CTTGGCCTCC CAGAGTGCTG GGATTACAAG 240 CATGAGCCAC TGTTCCTGGC CTCAAGCGAT TGTCTTGCCT CAGCCTCTTT AGTAGCTGGA 300 ACAACAGGCA CGTGCCAGCA TGATTTCGCC ATGTTGCCCA GGCTGGTCTC GTGACCTCAA 360 GTGATCTCTC TGCCTTGAGC TCCCAAAGTG CTAGGATTAC AGGCATAATC CACAGCACCT 420 GGCCTGAGTA CTCTATTTAA AATGCACTCC TCTCCTGTTA CTCTTGCTAT GGTTTTGTTT 480 ACCTTCATAG CAATTAGCCT CACCCGAAGT ATCATATTCT ACTCATGACT CCTCTGATGT 540 AAGCTCCATG AGGCAGGGGC TGTATTTGGG CCTTTGCTTG TTCCCAGTGC CTGGCATGGA 600 GTTATCTCTA AGTAAATATT TGTTGAATGT CTGGACGTGG TGGTGCATGC CTGTAATTCC 660 AGCACTTTGG GAGGCTGAGG TGGGAGGATC ACTTGAGCCC AGTAGGTTGA GGCTGCGGTG 720 AGCCGTGACG ACGCCACTAA ACTCCAGCCT GAACAACAGA GCAAGACCTC ATCTCAAAAA 780 AATTTTTTTA TTGTTGTTGA ATGAATGCTT GGAGAGCCAA AGGAGCTGAT TTAACCCTTC 840 AAAGGCATTA GATCAAACAG GCAGGGCCAG TTTTTCAGAT CTGAAAGGGT GTCCAGGAGC 900 TCTTCCCTCT TTCCAGCCCC TCAGTTCAGT TTTCTGGAAC AAGAAGGCAA CACTACATTT 960 GGATAATCAC AGCTTTTTCT CAAAGGCTTT TGACCCTGCA GTTGGTTTTT TGTTTGTTTG 1020 TTTGTTTGTT 1030
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