| Tag | Content |
|---|
EnhancerAtlas ID | HS108-42369 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:47795580-47796690 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chrX:47795631-47795642 | AAATCACAGCA | + | 6.62 |
|
| | 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 |
| GH0XI047935 | chrX | 47795272 | 47796731 |
|
Enhancer Sequence | AAGAGCTAAG GAAATACCAA AACAACCAAA TAAATTATTG GTTTAAAAAC AAAATCACAG 60
CATGGGTCAA CCCATTCCTG GGCCCTCTCC TAATAATATG CCTAGGACTA ATGTTCTTGC 120
CCTGCCTAAT TAACATTTTT CAAAGATTTT TAACTGACAG GATCACGGCC ACCTCACAGG 180
CAAGTACCCA AAAACATCTA CAGATGGTGT TGCTCCAGCA GTCAATCCGA GACCAAGAAA 240
CTCTCCGCCC CACCCCTCAG CAGGAAGTAG CCAGAAAGAA CACATCGCCC CTTGTCCTTT 300
TATAACTATA GGGTCTGCAA TGACAGAGCA GGAGTACTGT CATCTCAGAC AAACACCGCC 360
ACTTTCAGTT CCAGCTCCCT TTCTATCCTC ATGCATTTCA AGGAAATCAC TTCTCTCCTA 420
ACTGCAAGCA ACCAGAAAAG AGCAGACAGT AAAATACAGA TAAGACAGCT CAGGCACTGA 480
GCTGGGGCGG GCAGCGGCAG GGGCGGGCGG CGGGGGATGT CTCTTGGGTA ACTGCCAAAC 540
TTCACCGTCA TACAATGGGC CCCATGAAAC AGTGGGTCTT AATAAGCACA TTCCTTCCCC 600
TTCAGGTGCA GTAAGATAGG GAAGCTAAAA GCAGACTCTC CGGGGGGCGG GGGGAGGGGT 660
GCGGCGGTAT GCCTGCAGCT GCAGGAAGAT GTATGGGGAC AGACACATAA GTCTCCCTCC 720
CAGATAAGCA CAACTAAGAG ACACAAAAGC AGTCAAAGTC TCTGATAAAC TCTCCTGCCC 780
TAAATCCTTA AAAACTCTTA CCCCTCTCAG GTGTATTTCT CTAAAATGAA CCTGTCTTTG 840
ACTGTTGAGC CACCTTTCAT GTTTCTTTCC TCTTTCTTTA ATTCTTACAG TATACCCTTG 900
TGAACACATG AATGACTGGG AGCTGTGGCT CGCTACCACT GCCCAGCATT GTGAGAGACT 960
GTCATACCAC TTTCTACTCA ATGTGTCATG TTTACACCAT TGTAAAATTG AAACGTTGTA 1020
AGTTGGGGGA CCATCTGTAA TTGAAAACAG GTGTTCAAAG AAAAACTTGT ACACTTACAT 1080
TCGTAGAAGC ACTAGTCACA AAAACCAAAA 1110
|
