| Tag | Content |
|---|
EnhancerAtlas ID | HS059-49443 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chrX:119169300-119170480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chrX:119169650-119169663 | CCCCTGACCTTTG | - | 6.13 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH0XI120035 | chrX | 119169484 | 119170056 | | GH0XI120036 | chrX | 119170081 | 119170230 | | GH0XI120037 | chrX | 119170293 | 119171799 |
|
Enhancer Sequence | AAAAATGCAG ATTCACTGAG CTGACAAAGG CATAAGTAAC TATTCCTCTA CCCTTCTCTC 60
ACATGTAAAC TGTGTATTCA GTGAAAGGTT TATCAAACAC TCAAAATAAT GCAACCATTT 120
GTCTGTTATC TACCCACACC TTTAATTTTT TTTCCTTTTC CCCCAATATC TGCCCTTTTG 180
CCTTTAAATA CTGAAGTCCA CAAAATCTTC TTTGGAAAAA GGCATAGACC TGCCTTCCAG 240
ATGCATGTTC TTAACCTTGG TAAAATAAAA TTTCCAAGTT AATTGAGACC TAGCTCAGAT 300
ACTTTTTGGT TTACAAATTG GTAACCACCA AGGGATTCTG AGTGGAGGTG CCCCTGACCT 360
TTGACAAATC TTCTATTACT GCTTGGTACC AGCTTGAGAT ATCTTTATTG CTCAAATCAA 420
TAGGCAGATT TGCTGAGGCC TGGGAACTTC CCCCCTCCAG ACAATCCCTT GTAGCAGGAC 480
GAGCTGCAGA CAAAATCTTT CAGACACTGA GTTGTAGAAG GAAGGGCTTT ATTCAGCTGG 540
GAGCATCGGC AAGCTACTGT CTTAAAATCC GAGCTCCTCG AGTGCACAGT TTCTGTCCTT 600
TTTAAGGGCT CATAACACTA AAGATTTCAC ATGAAAGGGT CGTGATTGAT TGAGCAATCT 660
AGGGGGTATG TGACAGGGGC TTCATGCACC GGTAGTCAGA GTGAAACAGA ACAGAGCAGG 720
GAGTTTCACA GCGTTCTTCC ATACAATGTC TGGAATCTAT GGATAACATC GGTTGCTAAG 780
TCATGAGTTG ATTTTTAACT ACTAGGTTTA GGCCAGGCAG GCCCAGGCCT GGTTTCAGTT 840
CTGGTTTTGG GTCTGGTGCC TGGCTGCCTG CCCTTGGTTT CACTTCCTTG TTTTTTTCTT 900
AAAACAGGTA CTGAGTATAA AACAATATAA AACAATATGA GAGGGTCCGT CTCTTCCCTC 960
ACCCTGATCT CCCCAAATTT GGTCGATATC TAAGGTTTTT TTTTGCTGTA CAACTCCTTT 1020
TCTGGAGTTT TACTCACTTT CAACAAGGAA GGTGAGTTTT CCTGCTTCCA TGATGATGGA 1080
GGGCAGGCAA CTCCTTTCTG GAGTTTCAGC TCAATTCCAA CAGGGAAGGC GAGTTGGAGT 1140
TTTTTTCCTG CTTATAGGCT GGTAGAGAGC AGTGTTGAGC 1180
|
