| Tag | Content |
|---|
EnhancerAtlas ID | HS055-00390 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:96881130-96883400 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr1:96881353-96881365 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr1:96881353-96881365 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr1:96881351-96881366 | CTACTAAAAATAGAA | + | 6.57 | | REL | MA0101.1 | chr1:96882812-96882822 | GGAAATCCCC | - | 6.02 | | USF1 | MA0093.2 | chr1:96881296-96881307 | GGTCACGTGGT | - | 6.32 | | USF2 | MA0526.2 | chr1:96881293-96881309 | GCGGGTCACGTGGTCA | + | 7.37 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I096415 | chr1 | 96881221 | 96882960 |
|
Enhancer Sequence | GAGCTTGCAG TGAGCCGAGA TCGCACCACT GCACTCCAGC CTGGGCAACA GAGCGAAACT 60
CTGTCTCAAA AAAAAAAAAA ATAGAAGAAG AAGAAGAAGT AAGGTCATGG CCGGGCGCGG 120
TGGCTCACAG CTGTAATCCC AGCACTTTGG GAGGCCAGGG CGGGCGGGTC ACGTGGTCAG 180
CAGTTCAAGA CCAGCCTGAC CAACATGGTG AAACCCTGTC TCTACTAAAA ATAGAAAAAT 240
TAGCTGGGCT TAGTGGCGGG TGCCCGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGAAGA 300
GTCGCTTGAA CCCAGGAGGC GGAGGCTACA GTGAGCTGAG ATCTTGCCAT TGCACTCTAG 360
CCTGGGTGAC AAGAGCAAGA CTCCGGGAAA AAAAAAAAAA GAAAAAAAGA AAAAAAAGAA 420
GTAAGGTCAC CAAAGCCAAT AGGCCTAAAG GCAGACCTAA AACTAGCTGC CTCAATCAAA 480
GTAAAGTTAG ATGCCACAAC AAATAAACCC CTAATTCTCA GTGGTGTAAC GTGAGAACTA 540
TTTCTCCTTC ATGTAAAATC CACTACTCTT CCCACATATG ACTCATGTTC CTTCTGTCTG 600
TGGCTTCATC ACTTACAAGT GGCTTGGATC TGCTGGATCC TCTAATTCTG GCTGACAGAT 660
CGGAAAAATA GAGGGTGAAA GACTAAGTGT GAAAGTATTA CATGACAGGT CTGGAAATGG 720
CACGCATTTC TTTGGCCTGG AAACCACTGG CAACAACTTA GTCACACTTC CCTCACGTAA 780
ATGCAGGGGG ACTGGGAAAC ATAGATCCTG ATTTAGAAGG AACTTCCTAG GAAAATCTCT 840
GTACTGCGGA AGGGGAGCAT GCTCTGGTAG AGAGTTAGTC ATCTCTACCG CACAAGCCAA 900
ATCTAAACAG CTCAATAAGA CAGGCATTAC TGGAAGTGGA GCTCAGCAAG CTTGGACAAA 960
ATAAACCATG TGCCAATTCT TAAGCCAGCC AGAGACCAGA TGCCTCTGGC ATAGACATCC 1020
CTGCCAGTTA GGGCAAGATC CAGTTGATTA AGATACCGGA GTGGAATGAG CAATATGGGA 1080
AAACTGATCA ATCAGAGAAA AAAAATCCCA GCATGAAAGC CACGATTTTT CCCCCTCCAT 1140
TCCTCTCATC CAGAGATGGG CTGCCTGGCA CAAAATTCAA TCCGAATTTG AATTCTACTT 1200
AATATCAGCA ATAGAATTTT TCATTGGCCT TGTTCTGCAT TCAGTGATAA AAGCAGCACA 1260
CAATTATTTT CGATTGGACC AATGAGATTG TGCTGAGAAG TCTCTGAAGA CTGTCTGCTG 1320
AGTGCCAGTT GTTAATGAAT CCCATTTGTC TTTCTTGATT AAGTCTGCTA TTACCCCCGT 1380
TTAGTCCTGT CACCAACCCT TTAGCAAGAA TTTTCATATC ACTGTTTAGA TGAGAAATTA 1440
GCCTATAAGA GCAGCACTCA TCAATCAGGA GACAGTTTAT TTAATACAGT TTACAGTTTA 1500
TGAGTTCAAA AACTGTAGCC TCATACATTA GAAATGGATC CCTGTCCTAG ACAGACAATC 1560
AGGGGGTTCA GTTCACTTGA CAGGCATGGA GAAATGACTT TGAATGTGAG ATATGCACTT 1620
AGAGAAGGGC TGCAGTATCA CACGCCTGCA GCAGAGTATC AGGAGGCTTT CACTTCTGAT 1680
TAGGAAATCC CCTTTGGTTT AAGCAAGTGC TTCATTTTAA TACTTAACCA TGCCTCCCTA 1740
CAACACTGTG ACCAGAAAAT TCAAAATGAA ATTTTAGAAT AGAATCACTT CTTTGTGATA 1800
CCAAATCTTT ATTCTGGATT GCTATATCAT TAAAACAGTT CGTGAAGAAT ATTTATCTGC 1860
TTCTTGAAAT CATAAAGAGC AAGATATCCA TGAAAATCTT CCTTTTGCAA AGAGTAGTGA 1920
GTGGCATTTC CTTTCAGTCA CCAAAAGTAA AAAATTGCAG GAAAAAAGCC CCAGATCTTT 1980
GGCATTAACT GTATAGCTAC ATGACCATAC AAAATGGATG ATTTTGGCCC CCAGGAGAAT 2040
TTTAGGAAGC CCAAATTGGC AGAATTTGTT GGTTATTTGA TTGTATCAAA GACTGTGGCT 2100
GTTTTAAGTA TTCTATTTCA CATTATAAAG TATTGAACAA GCTAGATTTA TGGAATTGCT 2160
TTCCATAATA TTATTTCATT TGGGGCTATC ATTTTAAATT CATTTTACCT ATGACTCACT 2220
TTATTTTCCA AATCAATACT TTACCAACAC AGTGTCATTT GTATATATGG 2270
|
