| Tag | Content |
|---|
EnhancerAtlas ID | HS020-46744 | Organism | Homo sapiens | Tissue/cell | CD34+ | Coordinate | chrX:49100520-49101950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chrX:49100874-49100886 | CTCTGTTTACTT | - | 6.37 | | FOXP2 | MA0593.1 | chrX:49100875-49100886 | TCTGTTTACTT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGGGATTAC AGGCATGAGC CACCGCACCC GGCCCTAATC TTTCTCTGTT TCTGCACTTG 60
TCACTGATGT TCATTTTTCT GGTTTCTAGG TTTTTGCACA ATTTCTGCCT GTCCCCATTA 120
TTCTAGTTCT GTGTTTTTGC TGCTCCTCTT TCTTACCTCT CTGTCTCCTC GTTTCTGTAC 180
TGAATTCCTC TCTTGCTCTG TCTATCTATC TGTTCCCCCT TCTCCTCTGT CTACTTCTTT 240
ATCTGTCCCC TCTTCTTCTC TGTGCACCTT TTTATCTGTG TCCCCTTCTG CTCTGTCCAC 300
CTCTGTATCT CTCCCCTTCC TTGCTGTCCA CCTATATATC TGTCACCCCT CTGCCTCTGT 360
TTACTTCTTA ATCTCTCTCC TCTTCCTCTC TGTCCACCTC TGTATCTGTT GCCCCTTCCC 420
TCTGTCCCCT TATCTCTCCC TTCTTCCTCT CTGTCCACCT CTGTATTTGT CCCTCCTCCC 480
CTTCTGTCCA TCTCTTTATC TGTCCTCTCT TCTTCTTTTT TTTTGAGACG GTGTCTCGCT 540
CTGTCACCCA GGCTGGACTA CAATGGCATG ATCAGGGCTC AAGGCAGCCT CAAATTCCCG 600
GGCTCAAGCA ATCTTCCCAC CTCAGGCATC TGAGTAGCTG GGTCTACAGG TGCGTGCGCC 660
CGGCTAATTT TTGTATTTTT TGTAGAGATG GGGTTTTGCC ATGTTGACCA GGCTGGTCTC 720
GAACTCCTGA CCTGAAGCAA TCCACCCACC TTGGCCTTCC AAAGTGCTGG GATTACAGGC 780
ATGAGCCACC ATGCCGAGCC CCCTCTTCTT CTCTGTCAAC CTCTTTGTCC CCTCTTCTTC 840
TCTATCCATC TCTGTATCTG TCCCCTCTTC CCCTCTGTCC ACTTATCTGT CCCCTCTTCC 900
TCTGTCCACC TCTGCATCTG TCCCCTCCTT CTCTCTGTCC ACCTCTCTGT CACCCTCTCC 960
CTCTGTCCAT TTCTTTATCT GTCCCCTTTT CCTCTCTGTC CACTTCTCTT TTTCCCTCCC 1020
TCCATTCTGC TCTCCTATTT CTGTTCCCTC TTCCTCTGTG TTCACCCAGG TATCAGTACC 1080
CCTCCCCTTC TGTCCACCTT TACATCTGTC CCCTCTTCCT CTCTGTCCAC CTCTGTATTT 1140
GGCCCCCCTC CCCTTCTGTC TGCCTCTTTA TCTGTCTCCT CTTCCTCTGT GTCCACATCT 1200
CTGTCTGCCC CTCTTTTTCT CCACCTCTGT GTCGGCCCCC TCCTGGTCTG TCCACTTTTT 1260
TATCTGTCCT CTCTTTCTGT CTTCACCTCT GTGTCTTTTT ACATTTTTAT TTTTTTATCA 1320
TTATTATTAT TTTTTGAGAT GGAGTCTCGC TCTGTCACCC AGGCTGGAGT ACAGTGGTAC 1380
GATCTCAGCT CACTGCAACC TCTGCCTCCT GGGTTCAAGT GATTCTCCTG 1430
|
| |
|
|
|
