| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13584 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:120304290-120306860 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:120305690-120305711 | CCTTCCTCAGCCCCTTCCTCC | - | 6.38 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I119868 | chr12 | 120306177 | 120308793 |
|
Enhancer Sequence | GGCTTTGTAG GCCATTTGGT CTCTATCACA ACTACTCAAA TGCTGTTGTG GGCTGGGCAC 60
AGTGGCTCAT GCCTGTAATC CAAGCATTTT GGGAGGCCAA GGTGGGAGGA TTTCTTGAGG 120
CCAGGAGTTC AAGACCAGCC TAGGCAATCT CACAAGGTCC CATCTCTACA CAAAATTAAA 180
AAATTAGCCA TTAGTGGTGG CATGGGCCTG TAGTACTAGC TACTGAGGAG GCTGAGACAG 240
GAGGATTGCT TGAGCCCAAG AGTTGGAGGC TGCAGTGAGC TATGATTGTG CTGCTGCACT 300
CCAGCCAGAG TGAGACTTTG TCTCAAAAAA AAATAAATAA AATGAAATAA AATGCTGTTA 360
TGATGTGAAA GCAGCCATAG GCACTGTACA AACACATGGG TAGGGCTGTG TTCCAGTAAA 420
ACCTTCTTTA CAAAATAGGC ATCACAGGCT GTAGTTCCTT GACTTCTGAT TTGGAGACCA 480
CATAGAGGTG CCATGTGGAC AGCAAAAGGC CCTGAAACTT CATGAAGAGA GAGAGGCCCA 540
GCTGGGCCCA GCCTCCAAGC CAGGGCACCA AACACTGAGT AAGCCCTCTC ACACATTCCA 600
GCCCAGGAGA GCCCCAGGTG ACTGCAATCC TGGCCAATGT AATACAGAGC AGAGGAATCC 660
CCAGCTGAGT CCAATTAACC TACACACACA AGAGGTAATA CAATAACTTT TTTTTTTTTT 720
TAAGACAGAG TCTCACTCAT TGCCCAAGCT GGAGTGCAAT GGTGAGATCT TGGCTCACTG 780
CAACCTCCAC CTCCCAGGTT CAAGCGATTC TCCTGCCTCT GCCTCCCAAA TGGCTGGGAT 840
TACAGGCGCC CGCTGCCACA TTCAGCTAAT TCTTGTATTT TTAGTAGAGA CAAGGTTTCA 900
CCATGTTGGC CAGGCTGGTC TGGAACTCCT GACCTCAAGT GATCCGCCGC CTCAGCCTCC 960
CAAAGCGCTG GGCTTACACG CATGAGCCAC CGCGCCCAGC CACAGTGACT ATTGTTTTAA 1020
GTCAGTAATA TTTAGGGTGG TTGGTTGCAC AGCAATGTTG TACAAGGTGG GGTTTCTCAA 1080
ATTCAGCACT GTTGGCATTG TGGGCTACAT AATTCTGTGT TATGGGGGCT GCTTTGTGCA 1140
CTGTAAGGTG TTTGGTGGCA TCTCTGGCCT CACCCATTAA CTGACAGTAG GACCCTTCCC 1200
CCCAAACTCA CACACCACCA CCCCCAACTA GCTCTGACAA CCGAAAACGT CAAATCACCC 1260
ACTGGTTGAA AAACACTAAT GTAAGAGTAT GAAACTGGGA CACTAACAGC CAACTGCCTC 1320
ATCACATGGA AGTCAAGCAA AGTCAGAAAC AGGGTGAAGG CAAGGCCAAT ATATGACTTC 1380
ATAGGCCCTA GGTACTTTTG CCTTCCTCAG CCCCTTCCTC CATTAAAAAC AAAAAAGAAT 1440
TCAAAAATTA TATTTTATGG GGCCAGGCAT GGTGGCTCAC ACCTGTAATC CCAAAGCTTT 1500
GGGAGGCTGA GGCAGGAAGA CTGCTTCAAG CCTGGAGTTT GAAACCAGCC TGGGTAACAT 1560
AGTAAGACCC TATCTCTACA GAGAAAAAAG CAAAAATTAG CTGGGCGTGG TAGTGTGAGC 1620
CTGTAGTCCC AGCCACTGGG GTGGAAGGAT TGCTTGAGCC TAGAAGGTTG AAACTGCAGT 1680
GAGCCATGAT ATACCACTGC AATCCAGCCT GGGTAATAGG GCAAGACTCT GTCTCCAAAA 1740
AAAACAAAAA TTATATTTTA TGACTACATT AGTATAAAGA TGAATGTAAT CCAGAATCAT 1800
TATACATTAT TATATTCATT TTTCCTATAA TTTTAAAACA AATTAAAATT TAATTCAGTT 1860
AATTAAAAGT AATTAAATTC ATTAAAATTA AATATCACAG ATCCTAAGCA CCGTGCCTAC 1920
TCTGCCTAAT AGAAAGTCAG CCCTGAGTGA GTATAAGGAC AGGGCCACGG GATATTATTG 1980
AGGTCTCTGG AACTAGCTAT GCCTAAAGCT AAAACTTAAC TCATTCCTGG ATTTCTCAGT 2040
TTCATGAGCC AATAAATTCA CTCTTTTATT CACACAGGGT CTCACTCTGT CACCCAGACT 2100
GGAGTGCAAT GGCACAATCA CAGCTCATTG AGCCTCAACC TCCCGGGCTC CAGTGATCCT 2160
CCCACCTCAG CCTCCTCAGC AGCTGGGACC ACGGGTGCAA GCCACCATAC CCAGCTAATT 2220
TTTGTATTTT TTGTAGAGAT GGGGTTTCAC CATGTTGCCC AAGCTGGTCT TGAACTCCTG 2280
GGCTCAAGCG ATTCACCCAC CTCAGCTTCC CAAAGGGCTG AGATTATAGG TATGAGCCAT 2340
TGCACCTGGC CTAAATTCAG TCTTTGAATT AAGTTTGTCG CTTGCAACCA AGAAGCCCAA 2400
CTTACCTGGT CTCCCAGCTA TAAGAGGTGC AGCCTGAATT TGAACCTGGA TCTGTCTTAT 2460
ATAGAACCAG AGTTCTTACC GACTACTATC AACCAGTAAC TCATTCTGCC TCAAGCATCT 2520
TTCTAGTTTT TCTCTCTCAG GACAGTTTTC AAGAAAAAGT TCCCCAAACT 2570
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