Tag | Content |
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EnhancerAtlas ID | HS092-06639 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:70751700-70753620 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr10:70752609-70752619 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr10:70752609-70752619 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr10:70752609-70752619 | ATTTTCCATT | + | 6.02 | NFYA | MA0060.3 | chr10:70753579-70753590 | TCTGATTGGCT | - | 6.32 | NFYB | MA0502.1 | chr10:70753580-70753595 | CTGATTGGCTGCTTT | - | 6.51 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I068991 | chr10 | 70751557 | 70753663 |
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Enhancer Sequence | GATGATACAC TTTCTTTTTT ATGTGGGTTT TTTTTTTTGC TTGTTTTTTA TTTTTATTTT 60 TATTTTTGAG ACAGAATCTT CCTCTGTTGC CCAGGCTACA TAGCAGTGGC ACCTTCACAG 120 CTCATTGCAA CTTCCACCCT CCTGGCTTAA GCGATCCTTC CACCTCAGCC TCCCAAATAG 180 CTGGGACCAC AGGTGCCTGC CACCATGCCC AGCTAATTTT TGTATTTTTA GAGAGACGGT 240 GTTTCACCAT GTTGCTCGGG CTGGTCTCGA ACTACTGAGC TCAGGCAATT CTACCCACCC 300 CAGCCTCCCA AAGTGTTGGG ATTACCAGTA TAAGCCACTG TGTCTGGCCT TTTAAAAATT 360 TTTGCATGAC TTTTCATCTT TTTATGTGTG TTTCCCATTT GTTTGATATG AGGGAAAAAT 420 TTCTAATAGC TTGAGAATCA AGGGGATGGG GATTTTGGTT GTAGGCATTT TATAATAATT 480 AACCCCTTAG CAGTGGTGTA GAAAAATAGG TAAATTTTTT GTTTCAAGAC TTAAAACTAC 540 CTCAAGAAGA ACAATCTAAT GTAACAGTAT TTGTAACGCT TCCAGAGGTC TCAGATGAGG 600 AATTTTTTTG TAAATGGTTT GGAAGAAGAT TAAAATATCC TGGGTTAGCG TAGTAACATT 660 ACGGTAGGAT CCTTAGGTTG ATGCTGACTT TTGTTTGGGG TAAGTTTATA TTTTGTGTGG 720 TGTTTATTTA CTTTTTTTGA AGAGGAGGAT GTAGTAGGAG CAGTGTTACA AATCAGTTTA 780 AGTAATGGAG TAGACCCTGT TGTCAGTGGG GCATAGATGA GTTATGAGGG CTAAAGCTTG 840 CTCTGATGGT CTCTTTTTGT TTTGTTTTCT TTGCTTTTAT CTTTTGTTTT ACATTTGGGG 900 AGGGGAGAGA TTTTCCATTA AGGAAGGTTA TTGCTAGTGG ATTTGATTCC AAGGGTCTGG 960 GGTGTCACAG TAGGGTTGGG GAGGGGCTGC AGGGTGATCC TTGGCTACTG AACCTCCACA 1020 GAGAGCATGT GGTGCCCCTG CCCTTTCAAG ATAATTTACT CTCTTGTTAG TTTTGCAGGC 1080 CACCTCAGAT TCTCTGTTGA ATTGCTGTTA AGAAATACAG ACCAGTGTTG TTTCTGGGCT 1140 CTCGTTGGGT GAGGTTTTCC TGAGTTTTAT GTCTCTTCTT AGTTCACATC GTGTTACCCA 1200 GAACACATGC TTCACTGTCT TCTGAACAGG CAGTACTCCT GTGGCTCTGT GTCTTGGCTT 1260 GTTTAGTTTT TTTCAGCCTT GAAGGCTCCT TCCCACACTT ACTGACATCC ACTCATGTTC 1320 CTGGTATGAC CTGGATTGCT GCCTGGTCCC TGCAACCTCC CAATGCCCTT TCTGCTGCAT 1380 TCCCAGAGCA CAGGACTTTT CTCTTTTCTA CTGACCTTGC TTGGTTCTCC CTTGTGGGTT 1440 AGTAATTTCT GTCTGTCTCT TTGCCCCTCA CTAATTGTTC ACCCATGAGA ATTAGGTATT 1500 ATTCCTTTTA AATATACAGG GACCATATAG TCTTTATCTT TTATACATGA TACTTATTAC 1560 TCAATTTTGT GTGTGCAAGG TATCTGGCAC ATGGACCTGT GATTAGTAGC CTGAGGTCAA 1620 CAAATCTCAG TTAGAATGCG TAGGTTAAAC AAAGCTTTTT TTTTTTTAAA TTTAATTTAA 1680 TTTTATCTTT ATAGAGATGG GGTCTCACTA TATTGACCAG GCTGGTCTCA AACTCCTGGC 1740 CTCAAGTGAT CCTCACATCT CGGCTTCCCA AAGTGCAAGG ATTATGGGCA TGAGCCACTG 1800 AGCCCAGCCT AAACAAAGCT TTTAAAAGCT CCTGCAACCT CAAGGTTGTT AACCTGGTCA 1860 TCTCATGGTA ATTAGAAACT CTGATTGGCT GCTTTAGATT TCTTGATTAA AAACCTAAGT 1920
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