Tag | Content |
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EnhancerAtlas ID | HS133-18131 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:220545730-220547650 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr2:220545893-220545903 | TTTAATTACC | - | 6.02 | YY1 | MA0095.2 | chr2:220546396-220546408 | GCAGCCATCTTG | - | 6.74 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I219682 | chr2 | 220546781 | 220546930 |
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Enhancer Sequence | CCTGCCAGCA GAGCTTTCTT GATCACAAGA GACCTGAAAT AGAAATGGTT TAACCCTTTC 60 TGGATGATTA GACAAGGCAG GGGAGTCCAC ATCCCCAGTA TCTTTCCACT CCTTTCAGAT 120 GAATTTCAAA CAGGAGAGCT TAGAGATCAA AGAAGGATGC ACATTTAATT ACCCCACTGC 180 AGCCACAATC TGCTCAAACT GCCAGGAGGC CCCATGAACA TGAGCAAGTA GCAGCGCCAC 240 AGTCACCAGG CATAGATTTA TCAAAGTCTC ATGTGCTGGG CTCTCTGAAG GGTGTAGTGA 300 TTGAGAACTC AGCCCCTTCC CAGAGGGAGC TCAGATTTTA GTAAGCAAAA AACTGTAATA 360 AAAGATACAA CTGTGACCAG GGCCTTGAGC AAGCAGGGCA GTGACTATTC TTAGGCTGAC 420 CTAATAGCCG TTCCCTATCT CCTTCTTATT TTCCTTGTCT ACTCTAGGGG ACTTAAATCC 480 TCATTTCCTG CCCTCTGTTG CAACTAGTCA GTGATGATGT GGTTTGGGGT CATGAATTTT 540 AAGTGGAAGT CTGCTAGTGG GTTCCAGGAA AACTTCTGTT CTCCGGATTA AAAAGGAGGA 600 AGCAACTGGT CCTCCTACTT CTCCTTTATT CTTGCCTGGA AAGCAAATAT GATGCCTGGA 660 TGTGTGGCAG CCATCTTGCA ACCGTGAGGC TGAGAAACGG GTTCACCAAT AACCAGTCAC 720 AAGAGAGGAC CCCCAGTGCT TGGAGGACGG CAAAGACTAT CACTATGCCA ACCACCATGA 780 CTAGGATTCT GAACACTTCT GCCCATTGCA TTGCGGGCTG TAGTTTTACC AATTGCCTGA 840 GTCCCGTGAG ATAGAACAGA CTCACATGCA ACAAGTTACA GGAAATGGAT TTATTACTCA 900 GCAATAGTCA GCAAGGGACA AAGAAGACTG GGAGCCACTG TGAGCCAGTC CCCTAAGGAG 960 TGTGAATGTG TTCAAGAAAG CTGCCCAGGG TGGATGGAGT TTCCACTGCT TGTGCCCTAC 1020 TTTCATGGCA GCTGAGGGCC CCTAAAAGAT AGCTCATTTC CAGTTAAAAG CCTCAGGGGC 1080 TCCATGACTC ACCGAGCAAA GCTCGGAAGG ACATCCTACT TCCAGGGAAG AGAGGAACAA 1140 AGTGTGGGCT GTCCTGAACA GTTCCCTCTA ACTCAAGATC TTACATTCCC CAGGAGAAAC 1200 AGGAAAAGAG CCAAGCTCTT TCAGGCAGTC CTATCTCAGG ATGTTGCATT CCAGCACATT 1260 CTAAAGTTAT CCTGAGAACT ACATGCAGAA AGGAAGGGGC TAGGAACTGG GTCTTCCAAG 1320 TCCATCTGGG GACTGTACCA GATAAAGGCC ACTGTGGAGA TGCTGTCCCT GATATTGTCA 1380 GGCCCCCAAA GCAAAGTTGG CAGCTGCCTT CCATGAGACG ACCTCTTATG TGAGGAAAAG 1440 AAATCCCTAT TTATCTAAGC TTCTGTAGTT TTGTGTGCCC TGAGGCTCAA TGTAATCCTG 1500 ATACAGACAC GGAAAAGTAC AGATTAAGTG TCAGGGGGCT GTCCAGGTGG GACAGGGGAG 1560 TTGGCACAGG AGAGGTAAGG AAAGACTTCA TGGGGGAGGT CGTGGCATTT GAGTGGAGAC 1620 TTAAAAGACT TCAGGGTTAA ATATGTAGAG ATGGGAGGAG AGTAAGCCAT GGCGTGGGCA 1680 GAGGCTGATG TGGGAAGCAA GAACCGCTGG GGAAAAGAGG TGAGCAGGTT GCAGAAATGA 1740 AACCCAAGCC TGAGTGAACA ACAAATACTC GTGTGATTGG GAAGCCCAAG GCTGGACTCA 1800 CTTCAGACAT GTTTGTATCC AAGAACATAC ATTTTATCGT TGGGAGTTTG TTGCCTTTTC 1860 AGCTCTTCTT TCTGCCTTTG TCCTTGAAGA GCTGCCTTTG AGCAGCAGAT AGGATGACCA 1920
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