| Tag | Content |
|---|
EnhancerAtlas ID | HS141-14000 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr4:5034510-5036330 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr4:5034838-5034858 | TCCCCAACCACCAAACACCC | + | 6.23 | | RREB1 | MA0073.1 | chr4:5034845-5034865 | CCACCAAACACCCCACACAC | + | 6.81 | | STAT3 | MA0144.2 | chr4:5035083-5035094 | CTTCTGGGAAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I005032 | chr4 | 5034355 | 5036884 |
|
Enhancer Sequence | CTAACTCCCC ACTCCTCGCT CCCTCCAGAC CCTGGCAAGC ACCCTTCTAT TTTCTGTCCT 60
TTAGAGGCCC AGTTTGATTT AAAGGTTTAA ACTCAAACCA GACAGTTGAA CTCTCTGAGC 120
TCACAGACCG GCTCTTTCCC TTCCCAGCTG TGTGACTTTA TCTCATTTCT TCATCTATAA 180
AATGGAGGCC ACACTTTTAC CTCTCACATG GGGCTGAGAG AGGATTAAAT GGTCAATATT 240
TCCAAAGGCC CGAGGCTACT GCTGGTGTAA GGTAAGTACT GGAGATTTGC TATTATTATT 300
TATGTAACTT CCAGCCCCAC AAACACAGTC CCCAACCACC AAACACCCCA CACACTAGCC 360
TATAAGGGCC CCAGGGTCAG CGGCCTCATG GAAGGAAGAG AACGCTGGCG GAATGAGGGA 420
ATGAATGATG CCCTTGATTG CCTTTCCACT TACAACACGG TAGGTGATAC GGCGTCCACA 480
GCTGCAGCAC GGTCACCATA AACAAGCATT TCCCCAGCTG GGCCATGGCC CGTGGAAACC 540
CTGCTTCTCC CTCCAGGTTC CTGTGGACTC CAGCTTCTGG GAAGGTAAGG CTTCCTCCCT 600
TGGGAAGCAT TTTGAGTGTT TTGGCCTGTG TCCTTTCAGG AAGCCCCGTA GCCAACACAC 660
ACCCCAGGGC AGGAAGTGGG TGAGAACAAC TTAGACCTTG GACAGAAAGC AATTCGGAAA 720
CTGGCTCAGC CTCTTCTCGT TGCTGGCACG GCAAGCAGTG TTAAGTGTGA GCAATTTTTT 780
GTTTTGTTTT GAATTTGAAT GGTTCCTTTT TCTCCTTCAC GAGGAGGCCA TGGTTTCTGA 840
GAGTGGGGCT TGCATGTGGC AAAGAATAAG GATGGCAAGA AGGGCGGAAG CACCCCTGAG 900
CACTGCAGCT GCTACTTCCA GTGCACTCTC TGTTTACAAC CGCCCTGGGA GATGAGAAGA 960
AAACCTCCAG ATTATACTTG AAACGCTGAG GCTGGAAGAG GTAGACAAGA TGTGGCGAAG 1020
TCACACAGCT GCCAACTGAT GGGCTGGCCT GCTGGATCCC AGAGCCAACA TTCTTTGTGG 1080
TAGGGGAGGT GTCTAAACCA TCTTTTTTTG CTGGGGACAT GCAAATACAT GGAAACTCAC 1140
AACGGCTGTG TACTTCTCAC AAACTTTCAA AAGGTGTTTT GTGAATTGAG CTAAATTCAC 1200
TGCTGTGCAG GAGATGTGAG GCCCTAAACA TGGTATAAAA TTCTGTAACG GACACTTTAC 1260
AAAAGAAGAA GGAAAGGGAA AAAAGCAGAT TGAGAAATGC CACATACGTT TCCAGGCGGG 1320
GACATAGATT TCATGCCGTT ACACAGCTTT CCTAACTCCA TTTCACCTAG CTGGAGCTTT 1380
GGACTCTTAC GTAAAGTTCC TTATTCATTT GTTCAGCAGA GATTTATTAA GCAGCCACTG 1440
CGTCTCTTGC AACTACAGAA TCAGTCTTTT GAAAAATGAA CCAGAAAATG TATGGAAACT 1500
AATCCTGCCT TTCTCACCAA ACACACTGTA GGGATAACCT CTCTCATACG TGGGCGTCAA 1560
ATGTTTACAA AACTTGTGCC TTCCATCTGT CACTTTCCTG CTGGCCGCTG GGCCTCCGGA 1620
CACACAGTTC CCCTGCCTGC AGCACTCCAA AAATATTCTA TGCGCTCCCC TCCCTACAAA 1680
TATTTGATGA AGGAATAGCA GAAAGAACAC ATTCTTTCCA TGGTTTATAT AAGCACCACA 1740
CTCCTGCCAG GGCTATCTGT CTCAGCTTTT TCCTTTTCAC GATGAATCGT ACCACAGTTT 1800
GTGCCTGATG CTCTGCAGAA 1820
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