Tag | Content |
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EnhancerAtlas ID | HS002-02428 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr12:50636190-50637550 |
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) |
NFAT5 | MA0606.1 | chr12:50636565-50636575 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr12:50636565-50636575 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr12:50636565-50636575 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_00355 | chr12:50631329-50643885 | Adipose_Nuclei | SE_26085 | chr12:50633837-50637722 | Duodenum_Smooth_Muscle | SE_27814 | chr12:50633241-50637841 | Fetal_Intestine | SE_28691 | chr12:50632606-50637869 | Fetal_Intestine_Large | SE_34214 | chr12:50633704-50637749 | HCC1954 | SE_47348 | chr12:50633823-50639261 | Panc1 |
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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 |
GH12I050239 | chr12 | 50633140 | 50638182 |
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Enhancer Sequence | GGCAGTGGTG CAATCATAGT TCACTGCAGC CTTGAGCTTC TGGACTCAAG TGATCCTCTC 60 TACCCGGCCT CCTCCTGTTT CCTGGAACTA GGAATGGGTA AAGTTATAAC AAAAACAGGA 120 GAAGCTGTGA TAAGGTAGAG GCATGCTGGC AGGGGGTTAG GTTAGGGATC TTCATGCTGT 180 GATCATCAAT TCTACCATCT TGGTGTATGA CCTTCAGTCA TAATTGCTAA TCCTCAAGCT 240 CCTAATCTGT CAAAGGAATA GGGCAAATGC TAGCCAGACC AGTGGTTTCA AGCTCTGCTA 300 GCTGCAGAAC CCTCTCTTCA AATGCTGTCT TACGCAGAAC CTAACCTTTA CAAGGGATCA 360 AAGCAGGATT GCTGGAATGG AAAATCTAAA GAGCTGGGCC TGGGATCTGG GACTGGGATC 420 TGGGCCTGGG ATCTGGGCTT GGGTTTAGCC CTTAGGGTGT TCCAGTTGTT GGAGAACTGG 480 CCCTGAGATT CCTCTGAAGA CTTCAATTAA GATAGTTTAA AAACTACCAG GCTAGATTCT 540 CTTTAATTCC AAAAATGTAT GAGTCAAACA AATTCCACCC AAAGAGTCAA CTGTTATCAA 600 ATGAAGGATC ATATTATGCT GAAGTCAGTG GTGAGTGAAA CCAAAGCTAG CTATTCAAAT 660 GGATGTATCA ATAGGAACTT CTTACCTCAA ATTTAACGAC TGTTATAGAG GCTTAGTCAG 720 AGAAATAAGC CTGCAGCTAT AAAGGACCAT GGGACACAAG CTCTGATGCT AGAAAAAGTA 780 CTCTTCTATA CATATAAACA CAAAATGCAC TGTTAACAAT TAGAAAGTAA AGCTGACTTA 840 TCTACAAACA TCAGCTAGAT TAAGCTTCCT CCAAACAACA ATTTCATATT AATCTCTGAT 900 CAGAGACCTC CTAAGTTTTC CTACTGTTTT TAGCTAGGCT TGTATAGGAC TCACTATTTG 960 CAAACCCCAT AAATATAAAG CCACTAGGTG TTGGAAACAG ACATTAGTAT ATGCTTTGTG 1020 GAAAATAGTC CTGTAGTCTA CAGCCATACC ACCCTCAACG CGCCTGATCT CAACTGATCT 1080 CGGAAAATAG TCCTGCAGTC TTCTTTGGGA AGCTGCAGTG AGTGAACCTT ACAAACCTTA 1140 AGTAATATTA GCAACGTGTT TCCACTGAGT ATAAAACCTA GAACAGAAAT CCAGGCTGAT 1200 TCCCTGGTTT TCACTCCTTT CAGTATATAC CACCACCTGT CCTACTTCTA TGCCTTTACC 1260 TCCTGTTGCT CCCCTTCCTC TGGAATGTCT TCAGCATTCT CCAAGCCTAC CAAATAACTC 1320 TATTCATCTT TCCAAACCAG TTCCATGTGT TAAGCACATC 1360
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