| Tag | Content |
|---|
EnhancerAtlas ID | HS092-14468 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:43727090-43729300 |
Target genes | |
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 | chr13:43727639-43727660 | AGAGAAAAAGAGAAAGCTAAA | - | 6.22 | | IRF1 | MA0050.2 | chr13:43727712-43727733 | CAAAGGAAAGAGAAAGAGAGA | - | 6.39 | | LMX1B | MA0703.2 | chr13:43728896-43728907 | TTAATTAAAAT | - | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I043152 | chr13 | 43727073 | 43729513 |
|
Enhancer Sequence | GTAGAAGTAG ACGTCACTGG AGTGTAGGTG AAATAGAAGC CATGAGGGTT GAATAAAATT 60
GCTTAAGAAG AGCATTATAT TGGTTTCCCA GGGCTACTAT AACACATTAC CATAAAGCAG 120
GGTAGCATGA AACAACAGAA ATTTATTCTC ACACAGTTTC GGAGGCCAGA AATTTGAAAT 180
CAAGGTGTCA GCAGGGCTGT GCTCCCCCTG AAGTCCCTAA AGAAGGACCC TTCCTTGACT 240
CTTCCTAGCT TCTGGTAGTT GCTGTCCATC CTTGCCATTC CTTGGCTTCC ATCTGCACCA 300
CTCCTATCGC TACCTCCATA GCCACATGGC CTTCTTCCCT CTGTGCCTTC CTATCTCTGT 360
GTGCCCTCTC CTCTTCTTAC AAGCACATTG GTCACATTAG ATCTAGGGCC CACTCTAATC 420
CCATAGGACC TCATCTTAAC TATTTATATC TGCAAGATCC TAGGTCCAAC TGAGGTCACA 480
TTCTGAGGTT CTCAGTTGGA TCTGAATTTG GGGTTGGGGA GTGCTATTTA ACCCACTATA 540
ATGGTGAAGA GAGAAAAAGA GAAAGCTAAA GGCAGAATCA TGAGACGCAC GAACATTCTG 600
GTCGTTAGTA GGGAAGTGTT AGCAAAGGAA AGAGAAAGAG AGAGAGAGAG ACCACATTCC 660
TAGCTGCTGA GAGGCCGGGT GGGGATGCAA GCAGGTAACT GTGTGTGACC ATCAGAAAAC 720
ACTGGTAACG GCAGTTGGGT GACTAACTAA TATATTTCAC CCAGGACTAG AGTGGCAGTC 780
CAGGATGCAG AACTTTCGGT GCTAAAACCC AACAGTACCA AGCACACTGG AATGGTTGGA 840
CACTCTACCT GGGAACCAGC AGTTCTATTA GAACTGAATG TGGGGAGAAC GCACGGCTGA 900
AGCTTAATGG CTTGGGGAAT GAGTAAGCCT TAAGAAATGT ACTTGCCTGG GGCGTGATTC 960
TGGTTGCGTT GTTTTTCTGA CAATTCAACC ACATTTGGAA TTTTCTTACG TAGGATATGG 1020
GCTTGAGTTT TTAATTTAAA GTCTTCGGGT AAGGTCAGCT CAGTCCCTAA CCACCGGACA 1080
TCGTGGAACA ACCAAGTTAT TGGAGATTAA AGTGTCCTTC AACTGTCATG AATGCCACTC 1140
TGACCCTCCT TGTCTGGAGG GGACCTCCAG GGCATGCTAT TTAAATGAAC CCAATTTTGA 1200
AAGTTCACCT ATCTCTACTG AATGTGATAG CTATCTTGCT CTGCCTTCAG AGCACTTATC 1260
TTCAAAGTAT TCAGCGCCAG GCAAAAGCCT TGATTTTTCC TTGAAAAAGA AATTGTCAGG 1320
ATGTCTGAAT CCATCCAGAC CTTTGCATGT GTGATTTCAT TATTCATAGT CAGCATTCCT 1380
CTTCTGGCTT TTGATCTGTA GTTTACAGAA TGTGTGCATA AGGAGGCTCT CTTTCCCATA 1440
AACTGATCTC TTTACCCTCT CAGCCCGGAA TAACTTTCCA TTTATTCTTT TGATAAAGCG 1500
TTGATGCCGT GAGCCAGCAT ACATTAAATT TATCATGATA CAAACACAGC ACTACACTCT 1560
TATCCAGCCC AGATCAGCAA CCAGATCACT GCCAGTGCCC CTCAAGTGTC TCTGATGATG 1620
AACAGCAAAG GGGACCTGTG GAATTTCTCA CGACCATCAA ATCTGAAGAA GGAATTCTTC 1680
TGAGAGCAGT TTGCAAAGTC TATCACCAGT ATCCTGACTC TATTATTAGC TTGCAAGGTA 1740
GTTAAAGATA TCTTCTCAGC CTTGACTCAC TAATAAGCAC TTTTAAATAT ATATCAAAAA 1800
GCCCTCTTAA TTAAAATGCT TCAACTGCTT TCTACCTCTC TTCTGATAAA TGCCAATATC 1860
ATTAACATGG CTGCTCAGAA CCCTGCCTGC CTCTCCAGTC TTGCCTGGCC CCAGACTCCT 1920
CTTTCCCTTC TGCTACTTCC CCTAAGTTGA ATATTTTTCA TTCTTCTTTC ACCTGCTTAT 1980
CTCCTACTCA TCCTTCTCTT GTCATGTCAA TTATCACTTT CTTGAGGAAG CTTTTCCTAA 2040
CCCACCCCAT GTCCCATCCA CCTACTTGCC CCTGATCCCC AGGATACGTT AGAGACCTTT 2100
GCTTTCACAG AACTGCTACC AAGTCAAGAT AGGCTGACAT GTGACCATAG CAAGCACCAC 2160
CAAAACCTCA GGGTGGATGA ATGAGGATCC ACACTGCTTG AGACACTCAG 2210
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