| Tag | Content |
|---|
EnhancerAtlas ID | HS134-64843 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chrX:44173370-44174740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chrX:44173928-44173939 | CCCCATAAAAC | + | 6.02 | | SOX10 | MA0442.2 | chrX:44173934-44173945 | AAAACAAAGCA | + | 6.02 | | ZNF263 | MA0528.1 | chrX:44174392-44174413 | CCCCCTTCTCTCTCTTTCTCC | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI044313 | chrX | 44172418 | 44175535 |
|
Enhancer Sequence | CAAGATTATA CAATGTTCAT GATAATAAAT GAACACTCAT ATGCCCCACA GCCCTGCATA 60
AAAAATAAAT ACCTCAGAGA TAACTGAAGC TTTATCTCAG AGCTCATAGC CCTGCCTCCC 120
TTATCCAGAG GTAACCATTA TCCTGAATTT GCTTCTTTAA TGTTAGCACA CTGCCCAGGA 180
CTGTATATAG CCAGGGCAAT AGCCTCTTGC AAAACATGAT GCCTTGGCAG AGAAGTCTGA 240
TAAGGTCAAA AATACCTCAT TTCCTTTTGT GGTAAAGGCA GCCTGGAAGA ATGAGGAAGG 300
CCTGAGCAGC CCTCCCCAGG GGAGTCAGGG CCATAACAGC TGCCCTGGGC AGATAACAGC 360
CCAGCTCTAG GGCTGGGAGA GGAAAGCTAG ATGCAGTGGT TAGGATGGTG AGCTGTAGCT 420
GGCTCTGTCC CTTAGGGAAT CAATTGTCGC TACCTCCACC ATTCCCTCCA CTCTCTCTCT 480
CTGTCTCTCT CTCTCACACA TACACACACA CACACTTGCT CACACATACA ATCAGATTAC 540
CACAAGTCAG TCCCAGATCC CCATAAAACA AAGCAAAAGT TGGGTTTCAG AAAATGAATC 600
GTAGAATAAT ATAGAATTCA ATAATGATAT ACTGTCTCCT AAAGCAAGTA ACTCCGAGTA 660
ATCACAAAGT CACCTCGAAC CAACAAATGT TTCTTAAGTA CTTACTATAG TCCTAACTTT 720
GTGCCAAATA TACGAGTTAA AATAAGCATA AGACTCAGCC CCTGCCCTGA AGAAAAAAAC 780
CCACAATCTT GCGGAGGAAG CAAGATTTAG ATATATAAAA TGATACCGTT TGGATGTTTG 840
TCCTCTCCAA ATCTCATGTT GAAATGTGAT TCTCAGTGTT GGAGGTGGGG GCCTGGTGGG 900
AGGTGATTGG ATCGTGGGGG CAGATCTCTC ATGAATGGTT TCACACCATC CCCTTAGTGA 960
TAAATGAGTT GTCGCTCAGT TATTTCACAT GAGATCTGCT TGTTTAAAAG AGTCTGGGAC 1020
CTCCCCCTTC TCTCTCTTTC TCCCACTCTC ACCATGTGAT ACACTGGCTC TCCCTTTGCC 1080
TTCCACCATG ATTGGAAGCT TTCTGAGGCC CTCATCAGAA GCAAATGCCA ACACCACACT 1140
TCTTGTACAG CCTGCAGAAC CATGAGCCAA TTAAGCCTTT TTTTTTTAAT AAATTACCCA 1200
GCCTCACGTA TTTCTTTATA GCAACACGAG AACAGCCAAA TACAGCAAAC AACTAGAAAA 1260
CAGTACAGCT ACCATTTTTG ACCGCTTACT ATGAGCTGGA TGCTTTACTA AGGGTTTTAT 1320
ATCTCATTTA TTATCTCATT TCACTGTCAC AGAACTGTTT TAGCAGTGTT 1370
|
