Tag | Content |
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EnhancerAtlas ID | HS047-17273 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:23745610-23746880 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:23746787-23746802 | AAGGTCAAGAGATCA | + | 6.93 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGCTGGGGT TAAGTCGTGA GCCACCGTGT CTGGCCAGAT CTTCATCTTT GTATGCAACC 60 ACAACCATAC CTATGGCCCT ATGCCCAGAT ATTAGAGTCA ACATCTCTCC AATTGGCTGG 120 GTCCAGATAG TAGAGTCCTC ACTGCTTATG TTCTGGGTTT AGAACTGTGT CATCATTCAA 180 ACAGTGGTTG GATGCTCACA TATGACAGTC ACAATTCCAA CTATGGGCTG TGTTTGCATG 240 GGAAATTCAA GACCTCAGCA ATGGGCTCTT TCTCTGTGTG AGGGTGATAA TCCTAATGGC 300 TGGTGAGGTG TGCATATAAG AAACAAAATC TCACCAATGT GCTGTGCCCT GTGATAACAC 360 TCTCTCTAAC ACTTGAAGGC ATTATATTAT AGGTGGGGTT GTGGCAATCC TGTATGACCT 420 GCATACAAAG AGAGGACCCA GGATGTTGCT CATTTTTCTA AGTCGAGCTA TGAAAGACAG 480 TATCTTTTCT AATAGCTGAT TTGATTAATG AAAGCCATCA TCACATTTGT AAGCTGACAA 540 CAGTGTATGT CATAATTAGG TAGGGACCTA GCAGGAGAGT CACATCACCT GGATTTCAGC 600 CAAGGATATC TCACAATCTT CCCTGAGGGA GGCAGCCAAG CAGGAGTGTC ACATCACCTG 660 GGTGCTCAGC TAGGGATATG TTACAATTCT CTCCTGAAAG CACAGCACAG GCAACAGACT 720 CATGTCACCT GGGTGCTGAG CTCAGCACTA TGTCACAATG CTCGCTGGGG TCAAGACAAA 780 GACAGAAGAG CCACATCACC TGGTGTCTGG TTCCAGGGAT ATGTCACAAT CCTTCCTGTG 840 AAGGGGATTA TAAAATGTCA TATCTTCTAG GTCATGGATG CAGATATATG TCACAAGGTC 900 CCTGTGGGCA GAGCCCAGGC AGGAACATAC TATCCTATAG GTGTTGGGCC TAATGATATT 960 TTAAAATAAC CAAAATATGG GAGGCCCAGG CAAAACAGGA GAGTCACATC ACTTACATGC 1020 TGGGTCCAGT GATACGCCAC AATACCCCTT TTTGGCAGGG CCTAGGCAGA AGACCATTAC 1080 ATTGCCTAGT TGATGAATGA AAAGATATGT TATGTCCGGG CACGGTAGCT CAAGCCTGTA 1140 ATCCCAGCAC TTTGGGAGGC CGAGGCAGGT GGATCACAAG GTCAAGAGAT CAAGACCATC 1200 TTGGCCAACA TGGTGAAACC CCGTCTCTAC TAAAAATACA AAAATCAGCT GGGCATGGTG 1260 GCAGGCACCT 1270
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