| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13416 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:114601040-114603310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr12:114601725-114601739 | ATGACTCACTTCCC | - | 6.04 | | SPIC | MA0687.1 | chr12:114601680-114601694 | ATAAACAGGAAGTA | + | 6.43 | | SREBF1 | MA0595.1 | chr12:114601978-114601988 | ATCACCCCAC | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I114163 | chr12 | 114601469 | 114602237 |
|
Enhancer Sequence | ATTTTGGGTT CACGATTTGT GAAGATCTAT TTCGGGGTGA GAGGTGAGGA TCCGTGCATT 60
CATCTGGGCC CACCCATGAC CTGAGACAGG GGCAGGCAGG CATTTCTAGC TACAAGACTG 120
AAGCCTTGCT CCTGAGTCAT ACTTTAGATG CTGGGGACAG TCATCCTGAG ATTGTCTCTT 180
CCTGGACCAT ACATTACTAC TATTTTTTTT TTTTTTTTTT TTTTTTTTTT AAAGGTACTA 240
GGATAAGCAT CTCCCTGCCT ACCCATCGTC CCTGGGCACA AACTGCCCAG ACCCCTGTTC 300
CCAGTTAGGC CATGTTGTCA TGCCTCACAA TCACTATTCA GGACCAGCTG ATTGGGCTGA 360
GGTGACCACC TGACCCTGGA GCAGGTAGCT TACTGGCTGA CTGCTGAGGA CCTGGAAGAG 420
GAGGAGCTGG GTCAAGCTGG AGGTGTATTT AAGGACAAAA CCACACAGCA AGGAGGACAG 480
AAGTGGAAAG CTTCTTTTGC TATAGAACAG AGGTCAGAAG AGACTTGACC AGAGCCTGGA 540
AGCCTCCAAG AAGCCAGGCC TTCAAAGCTG CTTCAGTTCG ATTCAATTCC ACCAGGACCT 600
TTAAGACAAT TCCTTCTACC TGGGTCCCTT GAGGAAGCAC ATAAACAGGA AGTACACAGT 660
AGGAGGATTC TGTAGACCGG TACCCATGAC TCACTTCCCT CAGCTACACA GCAGGCTCCC 720
AGGAGTGTGG AGTACATAGC TGCCTTCCAT CCTGGTCAAC AGGGTGATGA GTCCATCCTG 780
ACTCATACTG TGGAGGACAA GCACATGAAG CACATAACTA AGCAGTCAAG CTAGGTTTTA 840
CGGTGACTCG AGTCTATATG GCCATTCAGG AGATGCCACT TGTGTTCAGT TTCCTTTCTG 900
GCTGTGGCTT ATAGAAAAGC ATCCTATTTT TCCCCAATAT CACCCCACCT ACCACCACCT 960
TAGTGCCCAG CTATAACTTG AGCATATAGC AATGAGTATC TGCCTCTATG TACCATGAAC 1020
ATCTTCATCC CACTTCAGGA AAGATGGAAT AACCTTATGA CAGACCCCAT CACACAGGTT 1080
TTTTCCACAT GTGTGCACGA TATAGGACGT TCCACTTTGT TTCCATGATG TATGCTGTTA 1140
TATAGCATAT TCTTTGCTTC CGAGTTATGA CCCAGTACTC ACGCAGTAGT ACTTGCTTCT 1200
TGCTCCCACT AACACACGAG TCGTTCTCCC CTGTGTGGCA CCAGGGGCTA AGTCAAACAT 1260
TAGCCCAATA AATATTGTTG GGGCCAGATG AAGTCATTGC CCTGAAGTTC ATGGACCTGT 1320
GTCTAGAAAC AGGTTCAGAA AACCCCAGGC CAACCATGTG TATCCCACAA ACTAGAAAAC 1380
CAGCAGGCTA GACTCCTTCA ACTGAAGGCT AGAAGTCCTC CAGGATGATT AGGCTTCATG 1440
TTCTTCCCAT TGTGATGGCC CTTCAGGGAG TTGCCAGATA CTAGAGGTAC TTCACTTTCT 1500
GAGTCCAGTT ACTCACTACC CTCAGTTCTC AGTTGTAGGT TGAAGGTTTC CTCTACCCTC 1560
TGAAGAATAT GTAGAGTAAG TGCCCCAAGG GTGGAAGCAT GCACCCCAGG AGTTGACGGT 1620
GGATTTTTTT TTGTGGGTGG GATAGGCATG GTCAAGTTGT TTTACTGAAG ATCATAACTT 1680
CAGGCAGGGT CAGACATTAA GTTCAAGACA TTGTTGTCCA AGACATTCTT ATATGCCCAC 1740
TTCATTTTTC CTTCATAAGG GCTATCACTA CCTGACATCG TGTGTTCATC CAGAACATTT 1800
CATGCAAGCA GGGACACTCC CACACTGCAT CCTCAGCACA AAGAATCTCT GTAGCATGGC 1860
AGGCATTCAG CGATCTGTTG GAAGGATTAC TCTACTACAT TCCTAGGCTA AGAAATTTGT 1920
TTTCATATCC TGTTTTAAGA TGTCTTGGAC TAGCAGCCTC ACATCTTGAG GGCTTAAAAG 1980
TTAGGCTTCA GTAGATTTGA AGCCATCCCC CTGATTCCAT AGTTCCTCAC CTCAGGCTCT 2040
GTAGTCCCAA GTTGAGATGT GAGCTTGGAT TTAAATACAG TATGTGGAAG GAGGCCATCG 2100
AGCAAGCAGT ACCCAGAGGG CTGGGGGCTT GGTCATCATT GCCTTTGGCA GCAGTTTGTC 2160
ATTGCTGGAT CACTGGAGGG CTAGCACGAG CCTGGGATGG GCTTTGATGT TCTGGTTTCA 2220
GGAGCATCTG TGCAGTCACC CACAGGTCAC CTGTTAGCCG GAGGAGTTCA 2270
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