| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29023 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:18806840-18808960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr2:18806969-18806980 | TTTGTTTACTT | - | 6.62 | | Foxq1 | MA0040.1 | chr2:18808499-18808510 | TATTGTTTATA | + | 6.32 | | ZNF263 | MA0528.1 | chr2:18807353-18807374 | GAAGGAGGAGGAGGAGGAGGA | + | 11.01 | | ZNF263 | MA0528.1 | chr2:18807350-18807371 | AAGGAAGGAGGAGGAGGAGGA | + | 6.87 | | ZNF263 | MA0528.1 | chr2:18807362-18807383 | GGAGGAGGAGGATTGGGAGAG | + | 6.88 | | ZNF263 | MA0528.1 | chr2:18807365-18807386 | GGAGGAGGATTGGGAGAGGAG | + | 7.03 | | ZNF263 | MA0528.1 | chr2:18807356-18807377 | GGAGGAGGAGGAGGAGGATTG | + | 7.53 | | ZNF263 | MA0528.1 | chr2:18807359-18807380 | GGAGGAGGAGGAGGATTGGGA | + | 7.67 |
|
| | 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 |
| GH02I018625 | chr2 | 18806839 | 18808864 |
|
Enhancer Sequence | TTCAATATGA AAATTTTCTT AAAGGTTGCA AATTTTATAG TTCCTCATAT ACCAAAAAAT 60
CTAGTTATCT TCTGAGCTAG ATCTTCAGCA AATAATAGCG TCCTGACATC TGTTTGCAAA 120
TGCTTTCTTT TTGTTTACTT GTACTAACTG TGTTGGTGAG AATTGGGATT ATTATTACAA 180
AACAGTGGTT TGATTCTTTT AGTCTAGTGA TAATGGAATC TAGAAGGAAG GGCAGATACA 240
CTGAAGGGAA AGTGAGGTCA CTGTAAATTT TGTAAATTAA TGCAATATGG AATTTTGGAA 300
TCAGTTCCCA GGGTGTAAGT TGATTAGACA CCGTAAGAAT ACGTTATTGA AATATAATAA 360
TGGATATATA GAAATTGGCA TGTATTTGAT CATTTGTTCT TATTTTTTGA CAATATTTTA 420
AAAGAGTTCT TAAATATCAT GTGCTAATAA TATAATTTTT CAGGTCTGAG TAAAAATATT 480
ACAAATTTAG GAAAATTCTA AAAAGAGAGA AAGGAAGGAG GAGGAGGAGG AGGATTGGGA 540
GAGGAGATGA AAAGAGAAAG ATAGAAATGC ATTAAGTGAC ACTTGGCCAA TGTCCAGAGC 600
AGCTACTCTA ACTTTAGCTT TTATCCTAAA ATCTCAAACT GAGAACAAAG AGCGTTTGAC 660
TGCTAACATC TCAGAAATAG GAAGGGATTT GAATCATTGA CTCCTGAAGA AGGCATGCCA 720
TTCTGGGAGA TGTCCCAGAC CCTTTAAGAA GGGCCCATGT ATCTGTTCAT CTGTCAGCAC 780
ACATTTCCCA TGTCTGTCTT TCTGTTCAGA ACAATGCTGT CCCTACTCGC CTGTTGTGTC 840
TTAACTGTTT TTATTGCTGT GGAAATATTT CAGAATTTGG AATATTTCCA CTTGCAATAG 900
TGTCATCTTT AAGAAATTTG AACACTAAGG GTACATGTTA TCTCCAGTTA TGATGAGTTG 960
ATTCATTGCC GGATGCTAGT TAGCCAAAGA TAGAAGCAAT TTTTATGCAA TTAATCATGT 1020
TTCCTGCAAA CTCTATAGTA GTTTTCAAAA AAGGTACATT ATATAAAACA TTTCATCCTT 1080
TACTGTAAGC TTAATGTTTG CAGAGTGTCT CTTGCTTCTT GGAGGAAGAC GTGGCATACG 1140
TTAAAAAAAA TGTAAATCTG TTAGTCCAAG ATTTTTACAA ACGAAGTAGA TGTTGCATGT 1200
GCAACCTAAA GGAAAATCAC TTGACATTAG TAGAGAGATC TATTTAAGAT TTGAGTATTT 1260
TTTGAATTGG AAAATAATCT CTAGTTATGC ATTTTCTCTT ATAAGTTTGG AGTTAGGGAT 1320
AATAGACTGT GTCCTGCATG GTGGAATCTG TGAGTGCCAT GGTTTGAGTG TGTCCCCTAC 1380
ATTTCATGTG CTGGAAACAA AATCCCCAAG GCAACAGTGT TGAAAGATGG GACCTTTAAG 1440
AGGTGATTAG GTCATCAGGA GTCTGCCTTC ATGAATAGAT TGATGCTGTT ATCATGGGAG 1500
TGGGTTCCTG ATAAAAGGAT GACTTTGGCC CCCCTTCCTC TTTTGCTCAC ATGCTCTTAT 1560
GCACTACCAC CATGGGATGA CACAGGAAGA AGGCCCTCAC AAGCTATGGC CCTAGATCTC 1620
GGACTTCCAG TCTCCAGAAC CATGAGCCAA ATACACTTCT ATTGTTTATA AATCACCCAA 1680
TCTGTGGTCT TCTGCTATAG CAACAGCAAA ATGGACTAAG ACAATGATCC AGAACACAGC 1740
CAGGCTCTGA GCCTGACCAA TGAGCCTCAT TCTCCAACTG ACCTTAGGTC AATCTTGTAC 1800
AAGTTAATTT GGCATGATTT AGTTATCTTC TGTGAAGTGC GAAAATGAAT TACATTCATT 1860
CAGGCACTAT TTATGGGGTG TTCACCATGA GTCACAAATG ATGTTAGGCA TTGAGGATAT 1920
AAAGATAAAT AAGATAAATT CACACCCCTC AGGAGCACAG ATGATAAGTG AAAATAAACA 1980
GGCCTCTAAT GCATGGGCCC AGTTCAGACT TTCTTCTACT AGCTGAGTGA TGCTGGATGA 2040
AGTACTCTGC CCTTTTGAGC CTGCTTCCTC ATCTAAATAT GGGAAGACAC TGACGATACT 2100
TCTCTGAGAA AGTTGTCACT 2120
|
