| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00288 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:25465830-25467410 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 | | Foxd3 | MA0041.1 | chr1:25466199-25466211 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:25466203-25466215 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:25466207-25466219 | GTTTGTTTGTTT | + | 6.32 |
|
| | 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 |
| GH01I025140 | chr1 | 25466725 | 25467101 |
|
Enhancer Sequence | CTGCTTTCCG TTCTTAGAAT GCGTCACACT TTCCCTCCTT TGCAAGTGCA GTTCCCTTTG 60
CCTGGAACAT CATTCCCTCA GTCACCTCTC ACTCCCGGTC CTCTTGCTAA CTCCTACCCT 120
TCCTGCACGC CTAGGCTTAA TCCTGGGAAA CCATTTGCCA CCCCCTTCCG CAAAAAGGCA 180
CAGGCTCCTG CTGCCAGTGC CTGGAGAGCT CCTTGTGTCC CACCCCAGCC CAGAGCATGT 240
CAAAAAGAAG AGATGAATGC CAATTTCCCA TAGTGTGGTC CACTGCTTCC ATTTTTGAGG 300
CAGAAAGTAA TGAGCAGTGG GTATCTAATG TGCCCTTAAA TATCTTTTTT TGTTTTTTTT 360
GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT TACCCAGCCC 420
AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC AGCTTCAACT 480
GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC AGAGCCATCC 540
ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT ATGTTGCCCA 600
GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC AGAGTGTTGG 660
GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA AAACAGACAT 720
TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC CCATCTCAGT 780
TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT CATGGTGGGG 840
AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA CTTGACTGCA 900
GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC CCCTAAAACC 960
ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT CAGCCCATTT 1020
CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA TACCCTGTCA 1080
TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG GAGGAAGTGA 1140
CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC 1200
CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC CCGGCAGGCA 1260
GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA GCCAAGATTG 1320
CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC AGAGCGCTGT 1380
GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC TACAAGCAGC 1440
TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC AGGGATGTTA 1500
ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC ATACACACAC ACACACACAC 1560
TCATCAATAT AGATGAGTAT 1580
|
