| Tag | Content |
|---|
EnhancerAtlas ID | HS120-04766 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr3:185140940-185143420 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLTF | MA0109.1 | chr3:185141401-185141411 | AACCTTATAT | + | 6.02 | | NFE2L1 | MA0089.2 | chr3:185141142-185141157 | ACTGCTGAGTCACTG | - | 6.71 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I185422 | chr3 | 185140456 | 185141947 |
|
Enhancer Sequence | TCATTATGTA TTACAATGTA ATTATAATAG AAATAAAGTA CACAATACAT GTAATGCACT 60
TGAACCATCT TGAAACCATC CCCCCTGCCT GGTCCGTGGA AGTAGTGTCT TCCACAAAAC 120
TGGTCCCTGG TGCCAAAGAG GTTGGGGACT GCTGCTGTAT AGGATAACCA AGAGTCCTGG 180
CAGCCAAGGC AGACCGGAAG TAACTGCTGA GTCACTGGCT AGGTCAGATA GTATGAAATC 240
AGCAGTCTTA AAAGAGATGA GGCAGGGCAA GGTCAGAGAG GCCAAAGGCA GGAGACAGCT 300
CAAGGTTGTG GCAGGTGATC AGCCAGAAAG TATAATGAGG AGATCAGTAA TGTCAAAGCT 360
CAGAGATGAG CACGAAAAGA ACAGGGGAGG GGAGGCTGGA GTGGGTGGAA TGGTGTCTGT 420
AACAAAGGGC TCCAGTTTTT CTTCTTTCTT CCCCCTGCCC CAACCTTATA TTCCCAGGGA 480
GCTTCTCAAG GCCTAGATTT CTCCATACCC TATAATTTAA GTGCCTCTTA ACCTAACCCC 540
GTCCAGTTAA AGTGATCTCT CTGGTTTGTT AGGAGGGAAG AATCACCTGC ACTGTATCGT 600
AAGCTTTCAG AGCCCACGTG TGGCAGCAGG AGTTACCCTT GCTGCACACT GCTCCCCCAC 660
ATTAGCCACT GCTGTTTCTG GGTCAGCAGC CCCATCACGC ACGCTCTGGT CATTCCCGCT 720
TCCCTGCCTC TGCCAGTGCT CTTGTTCGCC CCTGATTTCC TTCCGTCTGT CACACGCCTT 780
ACCTTTAAAG GTCCATCTCA AATCCTACCT CTTTTAGCAT TGTTCCCATC TCTCTTGGCT 840
CTGTAGAACG GAATATGGCT CACTTGTCAT GGGGGATGAT GGCAGGAGGT TATTCCTTCA 900
GTGTAATTAT TAGTTCCGTA AGTAGTCTGT GAGCTTCAAC AGGATAGGAA CCATGTCTTC 960
AGAGATTGCC TGGTACAGGA GAGAATGTCA TGATTAGGGA AAATAACCCG GTATTTCATC 1020
CCGGCTCTGT GACCTTTAGC ATCTACCTCT TTGTAGGCCT TCATTTCCTT CCATGAAAAA 1080
TAGGGATAAT CATTCTGTGT TCTGGATTCC TTACCTAGGG ATCAAAAACT TAGATCAAAT 1140
GATCACAGAT AACAGCATTT TTTAACCTGG AAAGCACTCT ATGAAAGTGA GGAGTCATAA 1200
AATGTTCCAT CGTGTTGTAA AAAAGGCAAA GGATTTGGGG AATCTGAACT TTGAGCTAGA 1260
TTTTAATTCC TGCTCTATTA CTTACTGAGT ATATTACTTT AGAGAAATTT CTTCTCTTGT 1320
GAAATAGAAA TGACATTATT ACAAGGATTA TGGTGCTGGA GCTGGCTTAT ACACCAGCTT 1380
TTAAGAGCCA ATTGTCAAAT ATTTAGAAAC TTTGCAAGCA AGTTGTTAAA CTTTTATTAG 1440
CTTGAAATCT GCTGTGGTGG GAATATTTAC ACCAGGGAAA TGAGCAAACA CTACAAACCA 1500
GATTGCTGTT GTTTTGGAAA GAGCTGATTT ACCAGTATAT TGCTGATTAT GTAAACAGCC 1560
TTCTGTAAAT TGTAAAGCAC TTTGTCTTAC TTATTATTAA AAATAGTAAT GGTAACAGTA 1620
ACGTTCTATA TCCACAGAAT CTAGGCTAGT GCATGGCACA ATTCTCAGTA TATATTCTTT 1680
TTTCTTTTTT GAGACAGGGC CTTGCTCTGT TGCCCAGCCT GGAGTACAGT GGCACAAACA 1740
CAGCTCACTG CAGCCTCGAT TTCCTGGGCT AAAGTGATTC TCCCACCTCA GCCTTCCACC 1800
CAAGTAGCTG ACACTACAGG CGTATGCCAC CATGCTTAGC TAATTTTTGT ATTTTCTGTA 1860
ATTTCTGTAT TTTTTGTAAT GTTTGTATTT TTTGTACTTT TTGCCATGTT GTGCAGGCTG 1920
AGTATATATT CAATAAACAC ATTTTGAATT TAGCTTTATG ATTTGGAAAC TTCTGCCCCT 1980
GTGATAAATG AGCCCCATCT TTATCTTTCT TCCAATCTCT CTCTACAAAG TGTCTTTTTA 2040
AAATCAGATA GCATCAGTAA AAGCCTAGCT CCCTAGCTCA GTGCATGATG CATAGTAGGC 2100
CTTAAATTCT GTATGTCCAT AGTTGAGCTA ATCGTCTTCT TTCCCAACCT TTCTTTCTGG 2160
CATTTCATAT CTCAGTTATT GACATTGTCT GTCTATTCAT TATTCCAAAT AAGTGATTTG 2220
AAAAGTCTTC CTCTCCCCTT TTTCTTTACC CACATCCATG TCTAATCAAT TACTAGATCT 2280
TACTAATTCT ACCTCTTAAA TCTTTCCTGT TCTCTTCACT GCCATTGCTA ACTGACTTAT 2340
TCAGGTCCAA GTCATTTCTT TTTGAACTGT ACCTTCTAAC TGGACCTTTA GTCTTTCCCT 2400
TTGAATCTAA CCTCTACTTC TATAGACGTG ATTTTAATTT ATCTGACCAG ATTACTCCCT 2460
TGCTTAAAAT TCCTTAATGG 2480
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