| Tag | Content |
|---|
EnhancerAtlas ID | HS092-32162 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:127136760-127139330 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr5:127138868-127138879 | TTAATTAAATT | - | 6.32 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I127801 | chr5 | 127137671 | 127138492 |
|
Enhancer Sequence | TTTGGAATGG GTGCAGAAAA CCAAACAGAG CAAAAGTGTA ACACTCACAG GGTGAGTGTG 60
ATCTGCTGGC GTGGCAGAGA AGAGAAAGGG GATTTAAAAA CCAGGGTGGT AGGAATGGAA 120
CACTGAAGAT GGGGTGAGGG TTCTTCTGGA ATAAGAGATG AGAGTTCTGA GGATGCTGAA 180
GATTAGGAAA TAACTTGAAG TATTAATAAG AGTTGCCTGG CAAAATATGT ACTTGAACCC 240
CTTTAAGTGA GAGTCCCATG GAAAGTTTGG AATTTCTGTT TGGAGTGTGC CTCCTTAATG 300
TAACACCTGT GGGACCTGAC CTCTATAAGA GTCTCCTGGT TTCCGTGCCT CCATCCTGAG 360
TGAAGTTTCC AAAGCATAGT CCCTGCCCCT CATCTTCTCT TCTCCCTCAC TCCCCTCTCT 420
CTGCCTTACA CTGAGCCTAC TACTAGAATG GAGCTGCTAT CTTTCTTTAC ATATCCAGTA 480
TTATTTGATG TTCTGTGATT TTGCTCACAG TATTCTCTTA AACTGGAATA TCCTTCTCTC 540
TTCTCTTCAT TCAAATAACT CTTTTCTGTC CTTGCAAGAC TCAAGTTATG TACCAACTTC 600
TCCCTTAGTC CCCAGATTAT TTTCTGTGGG TCCCCACAGC CTCCTTTAGA TACATCTATT 660
TGAGCTGTTA AAGTAAACAT TGTAGACAAA TTAAATTTAA CAGAGTTCAT GTGAGCAAAG 720
AATGATTCCT GAATTGGGTA GAAATCAGAA CCAGAAGAGG TTGAGAAAGC TCCATCCAGC 780
AGCATGAGTA GCAAGCTTTT ATAGGCAAAA CACAGAAGCA AAGTAAAGAC ATTATCTGTT 840
GGCTACCTAA GTTAGGTGTT TGCCTTATTT GGGTGTGGTT GGATCAGTTG GGTGCCTGTG 900
ATTGGCTGAA GCTCAGCTGT TTGTGACTGG CTGAAACCCA ACTATTTGTT ACAAAAAATA 960
TACTCCTAAG TTAGGTTTCA GTTTGTTAAG TAGGAACTCA AAATAGGGAG AGAACCTCAG 1020
GCCAATGGCC TCCTGCTTAT TTAACAGAGC TCAATACACT ACACTTTGTT GACATTATCT 1080
GTTTATATAT CCGTTACCCA CTAGACTCTA GGGACATTGA AGGCAGCACT AAGAATGTGT 1140
CTCTGAATGC ACTACACCCA GTACAGGGCT GGGTGCATTG TAGCTACTCA ATACATTTTG 1200
CTGAATTGCA TTGAATTTTA TTCTGATCAT GTCATTTCCT TAGTTCCAAA GCCTTGAGTG 1260
AGACATTGCT TGTCCATTAT CCCAGAATAA AGTCTAACCT CCTGACCATG GCATTTATCA 1320
TGTTGACAAT GGGGACCTGA CCCCCTTTCC TGCCTCATCT CCATCTCCAT CTGCGACCCC 1380
CAAGTGCACC CTGCATCTCT GCCCTAGCAG CTTTGCTTGT AGCTCCTTGC TACCCTGAAT 1440
GCCTGTCCCT GCCATTGAGT TTGCCAGACT TTCCCCATTC TTTATCAAGA TTGTTTTTTC 1500
CACGAAGTTC TCCCTATCAG TCCAGAAGTA ATCTCTCCTT CTTTGGTGCG TTCACAGCAC 1560
TTCTCTGTGC CTCTTTTCAG TCATTTGTCA CACTATGCCC CACAAGAGAA TGATCTGATG 1620
CAGCCTCTTT CTCAAGACTG CAAGTTCCTG GAGGAAGTAT GTCTGTTTAT CTTTATTCCT 1680
CCCACAGTGT CTGGCTCGAT GTCTTGTACA GATTTTATTG AAATGAATTG TTAAAGTGGC 1740
TAAATTAAAA ATAAAATTAT TTTGGCATTT GTAGGAGCAC CCTTTATATA TCAGGGAAAA 1800
TCACTTTATG ACAAAGAATT GTATTCTGTG AAGATGTCAA TATTACATCA GGCATTAATT 1860
TAATGAGGCT GACTCTTTCA AATATAACAT GCAAGTGACA AAAGGTAAGG ATCTCTTAGA 1920
GTGGAAACAG AAGGAAAAAA ATAGCAGAGA AAGAAAACAC AGTTGCTGGA AATTCCTATT 1980
TCACGTGAAA TAAAAAGAGT TTCTAAAGGA AACATGGTCT TAACATGAAA ATTAACAACG 2040
TAATGTCTTG GCTTGCTTTT ATTCAGAGTT CACTGCTCTA GAACTCAATA GTTGAATAAT 2100
ATGATTGTTT AATTAAATTG ATAGCTATGA AATGGAGAGG AGATGAAAGC CTTAACATTT 2160
CAGAGTTATC ATTTGCTAAT ACTTTGAAGA TTAAATTCTC ACCCCATTAA ATTTACTGTG 2220
CCTAGTCACA ACTTAGACTT CTAAAGAAAT TATTAAGGGT TACCCCTCCC AGTGCACATG 2280
TGGGCACCCA GGCTGAGCCA TCACCGGGCT AAGCTGCCCT GGGCATCTTT ATCACTCCCT 2340
CCCATGATTA CTTATCCGCT TAAAGACCTA CATGGGATAA AACAAATATT TGAAATGAAT 2400
GTTTATAATT ACTTAAAGAT ATCTGTTCTT GTTAGGGCGA TTTGAGTCAG GACTAGGTAT 2460
CTTAATAAAA AATTCCTTTT AAAATTAATG CCTTCCAAAT TATGGAATCC ATATGTTGCC 2520
TGTGTTTAGT ATTAGCGGGT ATAAGTGCTT AGCCCCATCT GTTCACTCCT 2570
|
