| Tag | Content |
|---|
EnhancerAtlas ID | HS069-04837 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr2:99452210-99454440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:99453714-99453733 | TGGTGCCACCAAGTGGCCA | - | 6.65 | | DUX4 | MA0468.1 | chr2:99454180-99454191 | TGATTAGATTA | - | 6.32 | | FOSL1 | MA0477.1 | chr2:99452393-99452404 | GGTGACTCATC | + | 6.32 | | JUND | MA0491.1 | chr2:99452393-99452404 | GGTGACTCATC | + | 6.62 | | Zfx | MA0146.2 | chr2:99453305-99453319 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 99452356 | 99452772 | | chr2 | 99452260 | 99453153 | | chr2 | 99453696 | 99454000 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I098835 | chr2 | 99451659 | 99453100 | | GH02I098837 | chr2 | 99453681 | 99453830 |
|
Enhancer Sequence | CAATTGATGA AGGAAAGTTC TTCATCAAAG AATTTCAGTT AGCAAGTGTA CAGTGAATGA 60
TAGAATTAGA AAAACCACCA CTTTGTGACA AAATAACAGA TCATCACCAG GTGTTAAAAC 120
TGTCAGGTGA AGGTTGGTGG AGGGACGACA GTGACACACC CTGAACCCAC TGCTCAGAAA 180
GCAGGTGACT CATCATGGGA TGTGACAACA ACCAGCACCT GCTTGAACCT GACAGAATCT 240
GGATCCATCG AATGATGTAC CGGGAATTGG GAGAATATAG GAAAGAGTTG AGTCACACCA 300
AGAGAAAGCA AAGCCAGAAT ATGGGACATT CTGCAGGACA CATGGCCCTG CTCTTCCTTC 360
AGATCAATGA CGTGAAACAA AGGGAGAGGG CAAAAGGAAA TCGTTATAGA TTAACAGACT 420
TAAGAAGCAC AACCGCACAG ACACAGACAC GATAAATGGG CGTCACTTTA TTCAACCCAC 480
AGGGTCCCAT GTGGTTTGCT CGCACTAATG TGCCTTAGTA AATGGAGCTG TTTTCCCCAC 540
AGTGATGGAT GAGAAGTTGC CGCAGACTCT CCCACAGGCC AAGCAGTACT TGCCTCTTCC 600
TCTGTGCTGC TCTCTAAAAA TGTCATTTGC ACTTCCCAGG CCTCATCATG CTCCATTCCC 660
AATCTTCCTT GCCTAGCATC AAAACCAGCA AACTGTTACC AGTCACTGAG GGCCAGCTCC 720
CTGCAAGGTG CTGGGAATAT CAAGATAAAA AGCACACCGT CTCCACTTTC CATGGGCTCC 780
TGTGACAGGG AGGACATCAG CAAGCGGACA GGACAATTCA TCCCAGCTTG CCCCTCTGGC 840
TGGGCTCCTG TCTGTGGTTG GAGGGGCCAC TCCCAGGCCT GTCTCTCCAA CACCAGAACT 900
GTGTGCTCCA GTCAAGAGAC AGGGGTGGAT GGGGGTGGGT GTTAGAGTTT CCCTGGGGCT 960
TGCAAAGTGA TGACATTGAA TAATTAGTAA TATTATCGCG ATAACATCTC GTTCCCCAAG 1020
AGTTCAGAGA ACCGCCTAAA AAAAATGCAT GCACGCCGGG CGCCGTGGAT CACGCCTGTA 1080
ATCCCAGCAC TTTGGGAGGC CGAGGCGGGC GGATCGCGAG GTCAGGAAAT CGAGACCATC 1140
CTGGCTAACA CGGTGAAATC CCGTCTCTGC TGAAAATACA AAAAAAATTT AGCCAGGCGT 1200
GGTGGCGGGT GCCTGTAGTC CCAGCTACTC GGGAGGCTGA GGCAGGAGGA TGGCGTGAAC 1260
CCGGGAGGCG CAGCTTGCAG TGAGCCAAGA TCGCGCCACC GCACTCCAGC CTGGGCGACA 1320
GAGCGAGACT CCGTCTCAAA AAAAAAAAAA AAATGCATGC ACAGTATATC CCTTCCACAC 1380
TTCACATGGT GCAATGTGAG TCTATTACAT TCCCTGCTAG CACCAAAAAC AATCAAAACC 1440
TAAATCAAAC CCAAAACTGA AAAAAAAAAA AAAAAAAGGT TCCAATCTTT CCTTTCCAGT 1500
CATCTGGTGC CACCAAGTGG CCAGCAAAAT TTCTACTCCT TTAAAAAACA GGCAAGGAGG 1560
CTGGGGAGGG GCGAGAGCAA GAGAGGGGAC AGGACACCAC TATTGGGATG CTCAAGCCTG 1620
GGACCCATCT CAGCGTGGTC TGTACCCCAA ACCTGAGGGA TATTATGTTC TCTGAAGAGT 1680
TCTATCCTTA AAGGGCCAGC GTTGTCTTAA AAAAAAAAAG GTAAAAGCTA GCATAGCAAC 1740
AAATCTGTTT CGTTTCCTCT TAGTCACAGG AATAACTGCT AGAATAACTG CAGCATATGT 1800
ACTGTAACTA TATTTTAATG AAACACAAGT TACAAAAATA AGGATTTCTT TACTAGACCT 1860
CCCCAGTTTT TTGTGCTTAT TGGGTCTGTT CTTTATGATA TTTTTGGATG ATTTTTTTTC 1920
TAAGATAGCA AGGAGCGCCC CCTCCCCACC CCCATCAAGT GAAAATATTC TGATTAGATT 1980
ACTTAACGTT CAACTTTAGA GAAATGCATT TTTCTAATAT AGCATCTAGG TCCTCAAAAG 2040
AGTTTTAAGT CAAGTTAAAC CAGGGCCCCT ATCCTGATCC TGTCACTTTC AGCTGTAGGA 2100
TGTTGGGCAA GTTCTAAATT TTATCTAGGG CTTATTTTGT CCGTTTATAA AATGGCATAT 2160
AGTACCTCCT CTCCCACAGT TATTGTGGAC TTAAACACAC ACAGCATTCT CCATCCCTAG 2220
GTTTGAAAAG 2230
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