Tag | Content |
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EnhancerAtlas ID | HS092-27646 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr22:46104610-46106840 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr22:46104739-46104754 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 46105053 | 46106237 | chr22 | 46104979 | 46105600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I045708 | chr22 | 46104701 | 46106651 |
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Enhancer Sequence | CCGGGTTCAA GTGATTCTCC CATCTCAGCC CCCTGAGTAG CCAGGACTAC AGGCGTGCGC 60 CACCACGCCT GGCTAATTTT TTGTATTTTT GGTAGAGATG GGGTTTCATC ATGTCAGCCA 120 GCCTGGTCTT GAACTCCTGA CCTCAGGTGA TCTCCCCGCC TGTCTCCCAA AGTGCTGGGA 180 TTACAGGCAT GAGCCACCGT GCCCACCTAA ACTTTTATTA ATCCATTGAA CTTTTTACCC 240 AGTTTCACTA CAAAAATGAA GTTATAACTG GGAGCAAAGC ATTCTTTTTT GTTAGTATTT 300 GGGTTATCTA GTTGATTTAT TTTGTATTCT CTAGGGATGT GTCTTGCCTT ATGCATGTAC 360 ATTTTATTAT CAGCTTAAGT GTAACAATAT TAGGAAGATA AACATAATTG TCCATCCTCT 420 TGCAGTCTGA ATCTGTTGCC CCTCTTCTGT TCGCGCACAA CAGCCATGCA TTCCACTTTC 480 ATGGCACTTA GCGCATTTAA TTGTCCATTA GACTGTGAGC TCCCTGTAAG GCAGGATTTA 540 GTGTTGTTTG TTATTGGATC TTTAACAAGA TAATATCTGG CATGTGATAA GCATTATTTT 600 AGTCATGATT CTTCTGAATC TAAGTGACTG AAGTCCACTT CAGATGGTTT ATGCACATAA 660 AGGGATTTAT TGGCTTATGC AACTGAAAAA TTCCAGGGTC ATTGGGTGAA GGCACGGTGA 720 ATCCAGGGCT GAAAGATGTC ATCAGTATCT GTCTCATCTT TGTCTCATTT TTCTCCTGTG 780 CTGGCTTTGT TGTAAGGCAC ATTTCCTGCT TCCTGTGTTG GCTCCTGTTC TTGCCTACTC 840 AGGGTTGGCA TGGCCCACGG CTGGTCCTCA GACCACTCTT CTCCATTATT GCTCATTCTC 900 TGGGTGACCT CATCTCATAC CACAGCTTTA AATACCTCTT CTAAATTGAT GATTTCCACA 960 TTTATGTTTC TGGCCTTGAT CTCTTGCTGA AGCTCTAGGT TTACATATAC AGCTTCCTAT 1020 TATGTGCTTC TAATTGGCAT CTGAAATGTA TGAAGGCTGC GTCCAAACTT TTGATTTCCC 1080 CCACACATAA CACCTCCTGT TACTCTACCA ATGTTTATCC TTCAGTAACT GGTACCACCA 1140 TTTACTCGTT TGCTGAGGCC TGGAACCTGA GTCCTGATTT TCTTTCACTC TCACCCACTT 1200 ATACTCATTA GCCCTATCTT CAAAAGGTGT TCCACATTCA CCTACTTCAT GCCTCCTCTG 1260 CCATAGACAT CTTTCATTGC TACTGCCAGA ACTTTCTTAC TCATCTTTCT GTCTCTCCTT 1320 TTGCCCTCTG AATCATCACA CAGTAGCCAG AGTGACCTTT TAAAAATTAC TGTAGCTGTT 1380 GTCACTCCTT GCTTAAATAA ACCATTCAGT GCCTTCTTAT TGCAACCTAG AAGCAAATCC 1440 AAAGTACTTG TCATGTCCTG GCGTCTGACT GACCACCTCA TCTTATTTCT TACTACTTTT 1500 ACTCCTGCTC CTTAGTTCCA TCTGGTCTTA CTGTTTTTCT TTGAATACTC CAAGTTTGTT 1560 CTGTCCTGAA TCTTTACATC CGCTGTCTTT CTGCATGGAA CCTTCCTTTA GATCTTCCCA 1620 TGGCTAGCTC TTTTAGGTCT CTGTTCAAAT ATCTATCATT TCGACTGAGA GACCTTCCCA 1680 GCACTTTATG TTCAGTAGTG TTTCCTGTAA ACCCGTATCG CTTTACTCTC TTTTATTCAT 1740 TTGTTTAATA GCACTTACCA CTATCGAACA TTATACAAAT CTTATTTGCT TTCTTGTTTA 1800 TTGTTGGTTG CTAGAATGTA GGACTAGCTC CATAAGGCCC TGGAGTTTGT CCTGGTCATC 1860 ATTCTATCCA AAGCACCTAG AACATGTGTT GACAAACTAT GGCCCATGGT CTGAATCCGG 1920 CCCACTGCTT CTTTTTATAA ATAAAGTTTT ATTGGAACAC AGCCAAGCTT GTTTATCTAT 1980 TGTCTACGGC TGCTTTCATG TAACAGTGGC AGAGTTGAGT AGTTGTGACA GAGACCATTT 2040 GGCCTGCAAA GCTTAAAGTA TTTCCTGTCT GGCCCTTTAT GGAAAAGTTT GCCAACCCCA 2100 TCCATTGAAG GGTTTTTGGT AGTAGTATTT GTTGAATAAG TCTGGTGATT GGTGGCATCG 2160 TTGTCCTTCA GTCACTTCAG GCTTATCTGA AGCAGATAAG CCTGGTTCTC CTGAACCAGA 2220 TAAGACTTTG 2230
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