| Tag | Content |
|---|
EnhancerAtlas ID | HS113-02060 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:115676960-115679320 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:115678990-115679001 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr1:115678990-115679001 | ACAGATAAGAA | - | 6.62 | | RREB1 | MA0073.1 | chr1:115677612-115677632 | GGGTAGGGGGTGGTGGGGAG | - | 6.4 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I115133 | chr1 | 115675635 | 115679109 |
|
Enhancer Sequence | AGTGCCACTA ATCCAGAGGC TTGCCAGTGG CATGGCTCGT TTGAAAAGAG GAGCCTGGCC 60
AAGCCACATT CCCCACTAAG GGCTCTGAAC CAGAAGACAC TGAGAGAAAG GACAGCATTG 120
GGACTGACGC TGCAGGATCA CGATGTTGCG GGGAGTGCAG CCAGGATGGG CACATGGAAG 180
AGCAGGTGCT CTGAGAAGCA GGAGCTATGA AGTGGGGGAA AGTGACAGAG AGTATGGGGA 240
ATCAGAGAGC CGTTCAGTGG TAAGGAAGGG ACAGAAAAAA TCGTTATCAT GTCAATGACA 300
GAACATTAGG TGGAAATGTA CAAAGTCCCA CTATCGAGGG CCTGAGGGCT GCTGCAGATC 360
CAGAGCCAGC CTCTGCGTGC TGCTCCCACC CCACTATGCC AGGCCGTTTG GCTTTCTCTG 420
GGTGCCCGGG TCCTTGCATC CTTCAAGAAA CCCCCATGAC AAGAGGAAAG CTTGGTTAGT 480
CTCAGTCTTA TGGAAACAGA ATCTATGCTA GCCTAAGTCA TTTCTTAGAG ATCTGGAGAA 540
TGAAAGTCAG TGGAACGTCC CTAGGCACAC ACACATGTGA GTATCTCAGT GTAAACGTAT 600
CTGCAGACTC CACCACAACC CAGAAGTCCT GTGAGTGTGG GGCAAGCATG GCGGGTAGGG 660
GGTGGTGGGG AGAGCGCCGA GTGTGGGGAG ACCGAGGGAT CAGGGAGGAA AGCACTGCCT 720
CCCCTTCCTG GAGAGTCCAG TTGGAAGAAC TCATGGGTCA TGGCAGTAGA AAGTGCTACT 780
TTTAGTTTCC TTCAGGATGT AGATGCCATT TAAAGTCAAA CTATTTCCTA ATACTGGTGC 840
CCAGAAAATG ATTCATTGGA GAATGCTGAT GTTGTTTTCT GTGCCCGACA TGAAGCAGTG 900
TGATGCTGTT TCAGAGCAGA GGATATTGGC CTGAAGGGCT GTAACTCTGT GCTGTCCCCA 960
AAGGCCGTTT CTGGGCAGTG TTTATCTTTT GTCTGCCTGA GACTCTCTGT GTGGCTCACT 1020
CTTCATCGTG ATTCTTTGCA TGCCTGTAAC ATGTGTCATC TACACGTATT CTTTTGGCAC 1080
CCATCACCTA CAGTTTTGGT TACTTCCCTT AGAGGCTTGT GTTTGTGTCT GGGGGTGTGT 1140
TACTTTCTTT GCTTCCCCAG ACCCTGGATC CATATTCAGG AGTCCCTGCT CTGACACTTT 1200
GTGCTATGTG AACTTCGACA AGCCACGAAC GTCCCCACAC TTCTATTTCC TCACCTGTAA 1260
AATGGGAATG ATGACATCTG ATGATAAGCA ACCATGGCCA ACTTATCTAA CAGAAATGAA 1320
GGTCCAATGC CAATATTGGA GAATGCTTTG TAAATTCCGA ATTGTAGTGT TCAGTGAGAA 1380
ATTGATAACA TTTTCTTCTT GTAAGGACTG TACTTCATAG ATTTTTAATG GCTGTCTCAC 1440
ATCGCAACCC CAAGATAACA CACTGCTGAG CAAATAGGAG GAGCTCAATA AATAATTGTA 1500
GAATGTGATC ATCGTTGTTC TCATCTTTAC AAATTCCTTA TTAATGCCGT TTTGTTGCTG 1560
CCAGATAACT CATTGTCTTC CCATGCTGAC ATTATATAAG TCTGGGACAC ACATGAACAT 1620
GGGAAGACAT CAGAAAGTTA CATAACTGAC CAGTAGAGAA TAAACATCAG TTACACATAA 1680
AGGTTAAGTG CATTTTAGAG GTTAGAAAAA GTGATGAGTG AATAATTGCG ATAGGAAAGT 1740
GGTTTGTGGG AACAGCTATA AGATATAGAT TGAGGTAGGT GGGATTGGGG AAGCTGCTTT 1800
TATCTAATTA AGAAGACCTT CAAGAGGAAG TGGATTTTCA GGAGCAGGTA GACGAGAGGG 1860
CAGAATGGGC TTGGTGAAGA GGTGGCCAGA GAACATTCCA GACACATGAG TATCCTCCGA 1920
AGGCTGTGGG GCAAGATACC TTCAGGGTGG TTTGCCCCTC TTGACAGTTG GAATGGCTAG 1980
AGGGGTGTGT GTGTATGTGT GTATAGACAT AGGGAAGCGG AGGGCAAGGG ACAGATAAGA 2040
AGGGTGGGAA AGAGGTAAGG GAGACCTGCT GGGGGTGATG AAGACAATGT AAGACTGATA 2100
ACCTTCAGGT GTGAGATGTT TTGGAGGAGC CCTGTTGAGA TTTCTTTACA CTGTATCCAA 2160
TAAAGTTGTC CTCAGCTTCT TTGTTTGGAT TCGGCACTTG GAAATGGGGC TAGTTTAAAA 2220
TCAGAGGGAG GGATAAAGCT AAGAATGTGG GCAGGGTAAA GAAACCAGGT CCCCAAATCC 2280
ATATAACAAC TTACAGACCT TATGCCATTT TAGTTAAACT TGGCCTAGCA CCTTTGGGTT 2340
TGAAGGTTTA TCATTAAATA 2360
|
