| Tag | Content |
|---|
EnhancerAtlas ID | HS002-06546 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr22:46362530-46365180 |
Target genes | |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr22:46363543-46363554 | CCCACCTGCCC | + | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I045966 | chr22 | 46362089 | 46369100 |
|
Enhancer Sequence | CTGCTTGGGG GAGCAGGACG TTAGTGTCTT CTGCACACAG CCTCAGACCC AGCCTCGTGG 60
CAGCTCCAGC ACCTCAGCTG CCACCTGCTC CAGCCTGGGG ATGGAGGAAG TGTCGATGGC 120
CCTGTGCCAA GCCTCACTTG CCACTCTACT ACTGAGACTG TGGGATGGCC TCTGGAAAGG 180
CCAACCACTC CACCGGCTGC TTGCACAGAG AACCTGTGAG CGCTGCTTCT CTGCCCAGGC 240
AGGGACCCTC CCCAGCATCC CCGGCCCTCA CTCCTGCATC TGCTTGTATG CCTCCGGGGC 300
TGGAGAACTC ACTGCCTCTC TGCCAACAGT GGAGCTGACC CAAGCCTCAG GACCCACGCT 360
CAGAGGACAA GAACGCCCTG GGTGAGGGGC AGGGATGGGG GAGGGGCCCC AGGCAGGCTG 420
AGTGGGAAGA CAAGGAAGGG GGGAGGGAGC GCACCTGTAC CCACCCCCAC CCTGCCGGCC 480
AGCCTGAGGT GAGGCCCCCA GCCCTGCGCC AGGGACGGAG GACAAACGGT GGTTTTGTCC 540
TTGGCCAGCG GGCGGCCCGC ACCACACAAT GACCCTTTCA TCAGGCTGAA GGAGCCCTGG 600
GCCGGGGTTT CATCTGACAA GGGAGGGCGC CCGGCCTCCT GTCCCTTTGG GAGGGGAGCT 660
GAGCCCCATC TGAGCCGGAC CCAAGGCTGT GTAGGGCGGC AGCCTTAGGA GCCTGCTACC 720
GCCTCTCCAT CTGCTGGGGA TGACAGGGAG CAGTGTGAGC CGTGAGGGCT TGGGCTCCCA 780
CTGCATGTGG GTCCTAGTTC TGGGGCTCCC ACTGCATGTG GCCCCTTCCA ATTGGGAAGT 840
CCTCCAGAAT GCACTGGCTC CGCACCCTGG CCCTGGGCCG ATGGCCTAGA CACCCACAAC 900
CGAGCCCTCT ACCTCATCCA ACACCGCTAT GCCACACCCA GGGTCTGTTA GGGTCCTCCG 960
AGAACAGAGC CTTGGTCCAC ACCCAAGCAG GGGCCCTGGG CTCCCCATAG GCACCCACCT 1020
GCCCTGCCAG GGTGACTCAA GCCTCCGGGG ATGTGGTGGG TGGGAGGGGA AGGGGCGGGA 1080
GTGTGACTTG CTTGGCCATT GTCCACTGTG TCCCCAGAGG AGCCCAGGGA AGTGTGTGAA 1140
TGAGGGAACA ATAATGTGCC GTCGGCGCCT CAAAAATCAC CAACTTCATG ATCATCACCT 1200
CGCCCCCCAT CAGCACCTCC AACTGCTGGC TGGAGCCTGA GGCCCTGGGA GACCCTGATT 1260
CCACTCCCCG TGGGACTGCA TAGGGGGAGC TTCCCTTCAG AGGCAGCGCG GGCACTGGGT 1320
GAGGAGCTGG AACTGGGAGG GCTGAACCCC TGGGATCCAA GGTGACCTTG GGAAACAGCC 1380
TCTTCTCTGG ATCCTGGCAT CCCATCGGCC CACCTCAGCA AGATGTTCTG AGCCTCCCTG 1440
GAGGGGAACC CCTGGTGAAT GTGTTTGACA GTATTGTTCC CTCTTCTAGG GGTCTCTTTC 1500
ATGTGCCTGT TTAGTCTGGC CAACTCCTAT CCATCCTTCA AAACCCTGTC TGAGAGTCAT 1560
CTCCTCTGGG AAGCCCTCTG AGATGCCCTA GGGGGTCCAC CACTCCTTCC TGAATGAACA 1620
CAGCCACTGG GCCTCCCTCT GTGCTGCCTG TGGCCAACCT CCCTGTTCCT GATAGCTGAG 1680
AATGGCCTGT CTCCTGCACA CCGACCACAC CAGGCATCAA GCTAGAGCTT CCCACAGCCA 1740
CCCGGTGAGG TTTGTGCTCC CGTGATCTGC ACTGGAGAGG GAAGAGCTGG GCCTTGGGAC 1800
ACAGCCAGGC AGTGAGGGCC CTGTGGAGTC AGGATGAGGA CCCAGATCTG AGTCACTATC 1860
ATGCCCTTTG GCCTCACGGG AAACCATGTT AGAAAACGGC GCATTATCCT ACAGGCCTCA 1920
GTGCACAACC GTGGAGTCCA GCGTCACCCC AGGACCTCCT GTCCTCCCTC TGCACACAGA 1980
CGGTCCAGGA TGCACATTCT CCCCTTTAGC CAATGGTTGT TGGGTCTCGT CCACCTGGTG 2040
ATGAGTTCTG GGGAGTTTCC TGTGATTAGG GAGGCTCCAC TTGCCCACCT CCAGTGGGGG 2100
GTCCCCAGTT GAGATCTCAT CAGATTTCCC AGCTTGAACC CCACATGCAC ACCCTCTATG 2160
GAACGTTCTA CACTTTCAAG TGCCAACTAC ACGTGGCCTG ATCTGAGCCT TGGGAGAGGG 2220
ATCACCATCC CAAGTGACCC ATGAGGAGAC TGAGGCCCAG AGAGGCTCAT GGACCTGCTC 2280
AGGGCACACA GCAGAGCCCC TCCCAGACCT GGATAGACGC AGACCCTCCA GGCTGGGAGT 2340
TGCCCCTCCC CCAAGGGCAA CCTGAACACG CCTGAGCCAC GGGGCGCATC CTGTCCCCAC 2400
ACGGGCCATG GTGCCATGGG AGTAGGCCTG GTTCATCTCC TCCCCCTCGA GGGTCATGGC 2460
CACAGCACTT CTGGGACTGT GGCTGGCACC GCTGACAAAG CCACAGCGGT GGAGCCGGGA 2520
AGAGGCCTGG CCTGGCGGGG CCGTGGTAAG TGCCCCCCCA CCCTGCCACA GCCAGGTGGT 2580
CGGTGAGTAA CCGCCCCGTC ACCCATGACT CACTTGGCTC CCCAGAGCAG GCGGTCACCA 2640
TGACAGGCTC 2650
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