Tag | Content |
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EnhancerAtlas ID | HS145-27666 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chrX:69439490-69440640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chrX:69439983-69439995 | AAGTAAACAGAC | + | 6.52 | FOXP2 | MA0593.1 | chrX:69439983-69439994 | AAGTAAACAGA | + | 6.32 | PHOX2A | MA0713.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.32 |
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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 |
GH0XI070219 | chrX | 69439598 | 69440570 |
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Enhancer Sequence | AGCTATTATT TGGAGGAAAG AGTTAAAATG TCATGCCGTA TACCTAAGTG TATTGTAATT 60 AGATTAAAGA GTTTCATTTA AATCATCAAA CCATAAAAAT AACAGAATAA ACTGAAGGGA 120 CTCTCAGAAG ATGGGCTCAG GATTTAGAGT CCCTCTGCTT GCAGTTCCTT TGTGGTCTAT 180 TCCCTTAAGA GAAAACAGTG GGGCCCTCCT CAGAGCCTAC AAATGTTTTT CCTTGGCCCT 240 GGTGCTTTCT AGGCAGAAGC AAGACTCCAA CCCAATGGCA CAACACTACC TCATGTGCAG 300 CAAAATCAGT GGTCAAGGTC CCTTAGCATT TGTTGAGCTG AAAAGAAATG AATGGGGCCT 360 CTGCTCAGGC ATCCCTCAGG TGCCTCAGGC CCAAGCTCAC TTCTATTCTG TCGCTGCATA 420 ACAAGAAAGT ACCAAGAGGG ACAAGGGAGA GGTTGGATGT AATGTAGATA GGGGAACAAT 480 TCCTTGTTGA GGGAAGTAAA CAGACCTTCA GACTCACTGC TGCTGCCAGG TCCACAACTG 540 TCACAGGGAA CTCACTCTTT TCAGGCCTCC ACAACATAAA CCACCACAGT CTCAAGGCAC 600 GATGTCTGAG GAAGAATTAA AAACATTGAG AGCCTACATG CTGGCTCCCA AGACCTGGTG 660 GCGCTTTTTC TCAACAACCA GTTTTCCTGT TTTCCCCAGT AACTGGAAGA AAACAGAGCT 720 TAGGGATGGC CTTGGACAGG GAACTGGTGA ATCAGAAAAC ACAGCAGTCA TGCTGATAGC 780 TAGAGGAGGG CTCCACCCGC TTTACAAACC AACTGCCTGG AGGTGAGCCA GGTAACACAG 840 CCCCAAAGCA TCTGTGCAAA CAAGTCCTCC CTGAAGACAA GCAGAGTCTG GGAGATGCCT 900 CACTCTTTAT CTCCGAGATC TGTCACACCA TATGACATAT ACAGGTCATT ATAGCACATG 960 GTGTTTGTAG AGGATTAGCA GTTCAGCAAA TGTGTCAACC TGACAAATCA CTCAGTGCTT 1020 TCAAGTGATC ACTACCCTGT TCTTTGGTTA TTTTAACAAA TGCTTATGGA GTTCCTACTA 1080 TGTGGCAACC ACTGTTCTAT TAGGTTGGTG CAACCTAATA GAACTACTTT TGCACTAAGG 1140 CTGGGTGCAG 1150
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