| Tag | Content |
|---|
EnhancerAtlas ID | HS038-23061 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chrX:46987900-46989240 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chrX:46988570-46988581 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chrX:46988570-46988580 | GCCCCGCCCC | + | 6.02 | | SP2 | MA0516.2 | chrX:46988720-46988737 | TCAATCCCCGCCCCCTT | + | 6.48 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chrX | 46987941 | 46987987 | | chrX | 46988600 | 46988657 | | chrX | 46988400 | 46988600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI047128 | chrX | 46988000 | 46989999 |
|
Enhancer Sequence | GTCCCTAGAA CCCTTCCATC ACTCACCCCA GAAATCTTCT ATCAGAAACA CCCGCCCTCC 60
ATTGTAGCCT CTCAGGCCTA AAATCTCAAA TCAAATTCCA ATCCTAGGCC AACTCCCCAA 120
CCCTAAGACT GCCTTTTCTG GGGCGGCTCT TTTTTCACAG GTGCAGTGAG GCCATCGTTT 180
CTGTACAGCG CGGAAAAGCT AAACTGTTCT AAATCTGTGA CTTTCGAATT TTTTAAAGCA 240
TCATATGCCT TTTAAAAAAC AGATAAGGCC GGGCGCGGTG GCTCACGCCT GTAATTCCAG 300
TACTTTGGGA GTCCGAGGCG GGCGGATCAA TTGAGGTCAG GAGATCGAGA CCAGCCTGGC 360
CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCCGGGCG TGATGGTGGG 420
CGCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCACGAGA ATCGCTGGAA CCCGGGAGGC 480
GGAGGTTGCA GTGAGCGGAG ATCGTGCCAC TGCACTCCAG CCTGGGCGAC AGAGCTAGAT 540
TCCGTCTCAA AAAAATAAAA AATATAAAAT AAAAAACAGA TAAGCGGGTA GGGAGCTACC 600
GGTGGAACTG AGTTTCCTCT TTAAGGGAAA CGAGGACAAG GACAAGATCC CGTCTTTTCT 660
GCACTCAGTC GCCCCGCCCC CAACGCAAGT AGGCATGTTT ATTGGATGAT AAGAGGGTCA 720
GTCAAAGTAA GGACCAACCC TCTACTGCCA AAAGACACAT ACTACTCAAG GGCCCCTGAC 780
TCAGACGTTC TCACTGGTCG GAAATGCCAT CAATCAAGTT TCAATCCCCG CCCCCTTCTC 840
GCGGAAGAAC TATGGGTGCT AACCTCTCTC TCAGGCCTGC TGTCAATCGG CTCCGCATCC 900
TCTAGTTCTG CACATCCCCG GCCATCAGAG CACGAACTTC TGGTCGGTCC GCCTGCCGTT 960
CTTTCACCTA TAGAGCCCAC CCTCTAAAGG TGTCCAAGCT GCTCCAAAGA ACAATTGATT 1020
AACCCAACGG CTGTCTTTGG CCCTCAGAAC TGTCACACCT GGCTCCGCCT CTTCCCGGAC 1080
ATCATCTGTT GCACCAGAGA CTGGCGGGTC TGGAAAGAAG CTCTGAGCCC ATCCGCGTTT 1140
CTCTGTTGGA CCCTGTCAGG TCTCTTGTTC CGTGTCCAAT GTCAGTCGGG TAGGGAGGCA 1200
GTGGGGCAGT CTTGGTTCTC ATCCCACCCC GGAGTCTCTG CGCAGCCACA ATTCAGGAAA 1260
ACAATCTGGA GGCGGGTTCA AAACACTAAG ATTGATTGAA CGCGCTGATG GTTTGGTTTT 1320
CTCCTATAGC GCTTTGGTAG 1340
|
