| Tag | Content |
|---|
EnhancerAtlas ID | HS073-00637 | Organism | Homo sapiens | Tissue/cell | GM19238 | Coordinate | chr1:84969360-84971690 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr1:84970206-84970224 | TTATTGCTTTCACTATCC | - | 7.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCAATGTAA CTCGCTTTCA CAATTTTCAA GCACCACTAT GTGCCGCATA TACTTACAGG 60
CACTAAGAAT ACATAAGAAC AGCCAGAGCC CTGTTGTTAT GGAGCTAACA GTTCAGAGAA 120
AATGACAGAC AAGGTGCTCT GTAGTAAAAT GAATAATCTT TTAGATGGTG ACTGGGTGCC 180
CACCTAAGGG AAGGTGTCTG AGGTGACATT GAAGCTGAGA TCTCAATGAC AAGAGATCCA 240
GCCAAATAAC CATCAGTGAG AAACAGCATT CCAAACAGTG AGGAAAGCTG AGACAAAGAC 300
TCTAAAACTG GAACAAGCTG CTAGCCCCTA AGGCACTGTA ACAATCACCA TCCAGGAGGT 360
TGAAACCCTG TAATCCTGGC CTATTAGTGC CCCTTCTCAC TCTCAAAAAT GTCCTGACCT 420
ACCTATGACA GTTTGTCAAG CACTTATGGT AAGTTCTATC AATTGTACTC ACACATAAAG 480
GTTAAAAGTA AGATTGTGCT AGTTTAAAAA TCTCACAAAA AAATCACCTA GCCCAGTCAT 540
TGATAAAACA GATACACAAC GTTAAACCAC ATTTAGCAAC ATGTCTAAAG AAAAGCTCAT 600
TAAAAAGTAC AAAAGGGGAT GCTCCCCTTC TTGCTACAGC CTTAACATCA GGCAATAACT 660
CCAAAACCAA ATCATGTCTG GTGCCTTTAA TGATCCCGAC CAGAACCAGA AGTCTACTGA 720
AGATTTAGGT AGGATCAGTT TTGGGGAATT AGGGGAGCAG CAGCTAGGGT TTTCAAAGTA 780
AAGCTCTTGG AGTATTTTAG CCTGAGAACC TCATGTCATT TTCTTTGGAG ACTAAAGATG 840
TACAATTTAT TGCTTTCACT ATCCCACCCC CATTTTTTTT TCTTGGTCCA TCCTATCTAT 900
GATAAAGGCA CACCTGAATG ACATTTAATG GTTACGAAAT AAATGATTTC GAGTTTCAGA 960
GCCAAATCCA GCCAAGACTG ACTAGAAACC ACTGTGATGA GGTAAGAATT GGGAGAGTAG 1020
AGAAATGGAT TCCAAACTGC AGTGAGGTCT ACAGCATTTC AAGGACTGGA CGTGAGGGGG 1080
ATCCCACACC AAGACGAATG AGAATTCCCT TCCCTTCTGA GTTGACCACA ACTGAGTAAG 1140
CTAGGTCCCT GACATTTCTA GTTAACAAAA CTAAATGGGA GACTCTCTCT CAGGAGGATC 1200
CTGCACCAAG ACGAATGAGA ATTTCCCTTC CCTTCTGAGG TGACCACAAC TGAGTAAGCT 1260
AGGTCTCTGA CACTTCTAGT TAAGAAAGCT TAGAGACCCT CTCAGTTCAC AAAACATTTC 1320
GGCAAGTAAT AAAGACTAGC CTGATGAGTA TAAAATCAAA TCATCTTAGG AACTGGCTGC 1380
TTTTAACAGG GCACATGATT TACATTCTTG TTTCTTTTTT TAACTGCAGA AGTGTTTCAC 1440
ATGTAGCCTG ACCTATTGTA CCAGAAAGAA GCCAATCCAT TTAGGACTGT AAAAATCAGG 1500
AAATACTTAG AACAGCACTT GAATGTCAAG TTATTCTATC AACACAGACA AAAGGCTTTT 1560
TCTCCCAAAG TACCCCAAGA CAAGGCCAAT ACTAACCAGA CGCCAAAATA AGACCAATAA 1620
TTACCCACAA TAATCATTTT CTCCGGCATG CGGACCAGTC GATATCCCCA AGGTCAAATA 1680
TGAGCAAACT GTGCCATAGG TATGAAATGC ACGCTTTGTT CGAGGTTGTA CGGGGCACTG 1740
ACCGGAACTT TACACTCCAG GATCGTTTCG AAAAATGCTT ATTCAATCCA CAGTTTAAGT 1800
TATGCAATAA TTCGCTTAAA AGTATGTGTT CAACGGACAA GAGAAGTTGA AGGTAAGAAT 1860
TTAATACTAA AGGAAGTAGG TTTGGGAAAG ATCAAATGGG AGAAAAGTCT GCTCTGAATC 1920
AAAAGTCGGA AAATACCCTG TCCGATGAGA AACAGGAGGC TGGCAAAGTG GGAAAGGAAG 1980
GGTGCGGACA GCGCGCGGAG GCGCAGCTGT TGGTGAGACC AGCCGAGAAG GCTGCCAAGG 2040
GAGGTAGAGA CGGAGGAGGA CCGGAATGTC GGCCACGGTT CAACCCAGGG GCCAGCCCGC 2100
CTCGGAAAGT CCTGGGGCGG AAGGGCGAAC TAATCGTCCC CCTAAAACAC AGCGTAGACC 2160
CACGCGGCGC CTGCTCTAAA GCTGGCCGCT CCCCGATCGC CGCCGCTGAG CGCGCGTCCT 2220
CTCCAGGGGA AGCGAGGGCC GGCGCGTGTC CCGCCCGCCC CCGCCAGCTG GGCCGCCGGA 2280
TCCCACCCGC CGCCGCCGCC TTCCTCCCGC CTCGGCCGCC CGCCCCCGCT 2330
|
| |
|
|
|
