| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49104 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chrX:9814480-9816320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chrX:9816304-9816318 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 9815244 | 9815511 | | chrX | 9815730 | 9815855 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI009844 | chrX | 9813030 | 9816238 |
| Enhancer Sequence | CGTGCCACCA CACCCAGATA ATTTTTTTGT ATTTTTAGTA GAGACGGCGT TTCACCGTGT 60
TAGCCAGGAT GGTCTCAATC TCCTGACCTC GTGATCCGCC TGCCTCAGCC TCTCAAACTG 120
CTGGGATTAC AGGCATGAGC CATCACACCC GGCCAATTAT TTTATCTTTT ATAGACATGG 180
GGTCTTGATA TGTTGCCCAG GCCGCTCTCG AACTCCTGAC CTCAGGCATG AGCCACTGCC 240
TCCAGTCTGT GTGTTTTTCT AAAGAATTCT TAGTGGCTAA GGAAGGTTAA GACCTTCCTA 300
TCGTCTCTTT CATCTTTCCC CAGAGATGAG CCATTTTGAA CATGGATTTG GCATCTGTGC 360
CGCCTCTGAG CCCATGCTTG GCTGATCTGT GGTTGGCGTC TGCCTTCCAG AGAATTCCTT 420
GTTTTCCCAC AGTCCCTTTG CAGCTGTTTC ATGGAGCACG GGGACGCATG CTGGCTGCTG 480
CCACCAGCTC TGATGGCTAT GAAGGTTTGA GACGAGTCTC ATAGGTGAAA TCTGGGCTCT 540
AAGACAGCCC ACCTTTTGAA AGGACAATTC AGCCACCAGA ATATCATCTT CGATCTGCTG 600
GTTTTCTCAT TTTGGTTTCC AAAAGCCTTT AGCCATTGTT ATTATTCCGT GCTTGTCTTG 660
GTGTTAGCTC AGTATCCATG AAACCCGACA AACCTCTTTC TAGAATGAGG CCGGCAAACC 720
AGTCTCATAA TGTTCAACCC CAGTGAAGAG GAACTAAACC TCAAAATTGT TGTACCACAA 780
ACTCTATTGG CCTTTTATTG GTGGGGATTT TGTTTTTATT ACAAGAGGGG TGACTGCTAC 840
AGTGGCCTTT CCGGCACCAG GCCGTGCCTG ACGGATGAGA ATGCTGTGTC ATAAACAGTC 900
TTTTGCAATG ACTAACCGTG CTGGGTTGGA ATGCAGTGCA CACCAAAGGA AGGTAGGACT 960
TTTAGTGGTT GTCACAATAG CTGTGCGAAT CCAAATATGG CTGGAAAATG TCAACATACT 1020
CTCCAGATTA TCAGCTCCGA CGAATGTAAG AGACATAGTG TTAGGGGGAT GTCTGGATAA 1080
GTTGAACTCT AATCAGAGGG AAAAGGGGGT TGGAGGAATA ATGAATGAGG GAAACACTTT 1140
TATTGGGAGA ATAGCTTGCA AAACGGCCAG TTGCATAAAG TGTCCTGTCC TAAGAAGTCC 1200
TAGTGTAAGC CTCGGCCAGT CCTAAAATAT GAATGAGACC TAGGACTTAT TTTACGTATT 1260
GCTGTTATCC TTACTAGCAC TTTTGGAGTC TGCATTCTGG TAATGCCTAA ATGCTTGTGC 1320
TGAGTTACAT GTGGAAACAG CTCTACACAA CATTCCCTAG TCTCTTGGAC ACTTACAGTG 1380
TTGGCCAGTC CTTTTCTCGT GATTTTTTCC CTCTGATTTA CTCGTGTTGT AACAAAGTTA 1440
TCACTTTTTT ATTGTTTCTC TTTGCTTTCA TCCTTTGCAT CTGTGGCTGC TCACTTGCTA 1500
TGCCCAGGGA AGGGGAAGAT GGAGAAATAG ATTATGGATA TGGCACTCCA GGGCCTGTTT 1560
ACCAACAACC TGAAAAGCTT ATATTCTCAG CAGGTCAATA CTCCCCATGT CTGAGGGCGA 1620
ATGTTGTGTG GATTAACAGG CAAAACATGT TGCATAGATT TGCAGATCCA CGTTTACAGA 1680
TTCCCCACTG TATACTGAGG CCATCGAGGA ACCTGAATTT GTGTATCCCT TGTGGCTATT 1740
GATATGTTGC TGAAGTCAAG TCAGGTATGT ATTGAAAAGC ATGGCCGGGC GCGGTGGCTC 1800
ACGCCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCGGGTG 1840
|
| |
|
|
|
