| Tag | Content |
|---|
EnhancerAtlas ID | HS092-19697 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:75766380-75768910 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:75767761-75767782 | GCTTCCTTTCCTTTTCACTTT | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I075732 | chr16 | 75766748 | 75768421 |
|
Enhancer Sequence | AGAAGTTCCC ATTTTAGAGA AATTTCTATG AAAAAAAATG CAGTAGTTAA AGAAATAAAA 60
AACTTATAGT GACCAGAGAC CATCACTTTG GAGGTAGAAT TCAAAGAATA CAAAACCAAG 120
GCAACACAGG ATTCCAATAA ATACAAGATA CCATGACAAC GTGGAATCTT TGTTCTTAAA 180
GGGCCTCCAT GGATATAAGA TTTTTAGATG TAGGAAGATA TTTTCATTGA GTTCAACTAT 240
TTACTCATAT ATATGTTTTA CTCTTGTAAC CAAGTACCCT ACTTTCTTAA AAAAATACCT 300
TTACCATTTC TTTTTTTCTT GTGTGTTCAC CTCTTACTTA AGCTCCTTAG GGATGCAATG 360
ATAACCTTTA CCTTCTCTCC ACCAGGCACT TCCTGCATGG CAAGTTTATC TTACTAAATG 420
TTTGCTTAGA AATTCTAATG ACCAAATGTT GAACCAAACC AGGCACCCTC TGGAACTCCT 480
CCCGACCAGG AGAATGCATA GAGACAATGG TCAGTTTACA ACCTAGTTCT GGCCAGATGG 540
TGCCAGGCAG ACCATCCCCT AGCTAAGAAT AGAAGCCAGT CACATAGACC CTGCACCTCC 600
TCGTGCCCCT CCCCTGCATG CCATTCATGA CATGCCCCCC TTTAAAGCCC CTGCTTTTTG 660
CCCCAAAAGA TGAAGTGGTT TCCTTAAGGG AGGAGCCTGT ACTGTTTCCC CTCAGCTAAG 720
CTCTGGAATA GAAGTCACTT TCTTTTACCA CCTCATGCTT GTTATCTAAA TTTACAAGAA 780
GCTGAACCTG CATTCAGTTA CAATTTTGGT GGCCCATACA GGGACTGTTG TGTGTTCCAG 840
GGGCCTGAGC TTGCTGGTCT GGTTTCTACT GGAGAGGGCA TATGGCTGCC TGTGAACACC 900
AGCTGCTTAT GGCTAGCTGA CCCCATGGCT GGAACATTAG GAATTTCTCT GAAGCTGCCA 960
AGATGCTTTT GTTTTTGGGA AACTGTCTTT CACTTCCTGG CATGATGCCT GCGGCTTTCA 1020
AAGCTTCGTT GGTACAAAGA AAATGAACTC TGAAGAAGGC AAACTTTGGA ACTGGGTGAG 1080
CAAGTTGGAG TGTACCTGAC CACCCCCTGC CTCTTTTGGA GTGTTGCTGT GGCTCTGTTC 1140
TATTTAGATT TGGCTGCCAG AAACAACATT TGAGCTTTTT CTGCATTTGT GTTTGTATGT 1200
GAATCACCCT TGAGGCATGG CTTGGTTTGG ACTCGGTCAT CTGGAAGAGC TATTTGGAAC 1260
TGAGGCAGGA GATTTAGGAC TAAACCCAGC CTCTTAACTG GGGATCTGTT TGGAAGCACT 1320
CCATTTGTTC ATGCCTTTGT GTATACTCCA TTTGTATGAC CTTTGTGTAT AGGCCCTAAT 1380
TGCTTCCTTT CCTTTTCACT TTATCTTCCT GATTATCTCA GAGAGCCACC TACAGCCTTA 1440
ATCTTCTTGG CCAAAGGCAC CCTTAGCTCT GTTTACCTTG ACCAGTGATT TACGGAGGTG 1500
GGAGGGATTC ATCCCACACC GTGCAGGTCT AGGATACTGT GGCTCTTCCT GATGGGAGAT 1560
AAATGGGAGT GGTGAAGGTA CCGCCCACAC ACCACTTAGT GGCTTTAAGG CTCATAAATC 1620
TCCTTTTCTT TCTTTCTCTT CTTTTCCCTT CCTTTAAAGC CTGGCTCCTT TGCTGAGGCC 1680
TGCCAGGAAC TTCATACTCT CATCCTCTTT GGGATTCCAG CTAGTTACAT ATTATGACCC 1740
ATTTTTAATG CATGTTTTAA ACGGATGGGC AAATTATAGC AAGAAAAATT CAGAGCTCAA 1800
ATGGTTAGCC CGTAACTAAC TGCAGAGTTA AACAGAGTCT TCTAAAGCTC TCTATCTTCC 1860
TCTCTTTTCT TTACTGTCTG CTTTGAATCT GCTGTTACTG AGTTGCTGGT GCTGAGATAA 1920
GACTCATTAT TTGTGCTCTA AATGGAATGT AAACATTGGA AATTTGTTTG AAACGGAAAG 1980
AAAAATAAAA GAATAAAAGA GACTTTAAAA AAAACAAACT GCCATAGAGA CTGCTTTACT 2040
CAAATTTTGT TTTATTTATT TATTTATTTT TTGAGACAGG GTATCACTTC ATTGCCCGGG 2100
CTAGAGTGCA GTGGCATGGC CATAGCTCAC TCCAGCCTCC ATCTCCTGGG CTCAAGCAGT 2160
CCTTCTGCCT CAACCTTCCA AGTAGCTAGG ACTACAGATG TGTGCCACCA TGCTCAGATA 2220
GTTTTAAAAA ATTGTTCGTA GAGATGGGGT TCTTGCTACG TTGCTCAGGC CAGTCTTGAA 2280
CTCCTATCTC AAGTAATCCT CCTGCCTTGG CCTTACCCAA ATTTTGGTTC ACAGTTTTCT 2340
TTTTTCTTTT TTTTTTTTTT TAATTATACT TTAAGTTTCA GGGTACATGT GCACAACGTG 2400
CAGGTTTGTT ACATATATAT GCATGTGCCA AGTTGGTGTG CTGCACCCAT TAACTCGTCA 2460
TTTAACATTA GGTATATCTC CTAATGCTAT CCCTCCCCCC TCCCCCTACC CCAAAACAGG 2520
TCCCAGTGTG 2530
|
