| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18795 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:106226980-106228450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr4:106228197-106228207 | ATCAAGGTCA | + | 6.02 | | TCF3 | MA0522.2 | chr4:106228180-106228190 | AGCAGGTGTT | - | 6.02 | | ZNF263 | MA0528.1 | chr4:106227914-106227935 | GAAGGAGGAAGAAAGATGAGA | + | 6.06 |
|
| | 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 |
| GH04I105306 | chr4 | 106227483 | 106227804 |
|
Enhancer Sequence | ACTGAGACAC AGAATATCAA TAATTTTCTT AAAACAGAGC TAATAAGTGG CTCCAGAGCC 60
TGGTAGAAAG CAAGGCAGAT ATGAGGAGTT CTATTCTATC AGGGCAATAG GATGTTGGGC 120
TGCCCAGTCA GAACAGTGAA AAGCCCAGTA GGCCAGCCTT TCCCCCAGCT GTCCAATTTT 180
TTAATAGAGC TCCTGGTGGC AACATGTAGA TTAGCCTTAT TTAGACCTGT CAGCAAAGTC 240
CTGGGGATCA TGTCTGGGCC CCGTTAATAA ATGGCTAAGA TACACTGCCT ACCATTTCTC 300
TGTTCCACAG AAAGGGGTCT GGGTCAGTGA GAAAGAGAGT GGGAAGGAAA AGTCAAAAAC 360
ATCCTCAGTT CCAATGACAC AGCTTAGGAT GGTGAGTATA TGTCACATAC ACATTAAAAC 420
CCCCCTAATT AGGTTGTCCA CTTCTGACTC GGAAAAGCCT CAGTGGAAAA CATTATGCCA 480
TGATGCTACA ATACCTGGGA TTCTGCTCTG TTCAGCACTT CCAACCTTGA AGGACAAAAG 540
CAAAACAGTG TGGGTGTAGG TGGGTGTGTG TCTGGCTGCA AGCACATGCC AGCCACTGCT 600
GTCACACAGC CTTGCCTATG CCTTGGTATA TTAAAGAGTG GTGAGTCACT CACACTTATG 660
ATAACCATTC ATAACTAGAA TTTTAGAAGA GGGGAAAACC CCAGGGCTGT ACAGAATGAC 720
ACGTGACACT CTCCAATGGA AGGACAGAAA GAGCAGAAGC CTCTTGCTAA ATCTAACCAT 780
GAGCTCTTTC AGAGAAAAGA GGGCCGTTCA GCTTTTCTGC GTCACTATTA ATGTGAGCCA 840
GCTGGAAACA GAAAGAATGA CTCAAGAGAG TACTACCTAT CCTGGAAATG GGGTCAAAGC 900
AGGTATGGTG GGGGAACTGG TTGTGGGCGA GACTGAAGGA GGAAGAAAGA TGAGATGTGT 960
GTTTCCTCAA AGTTGATGCT CCTCTCAGTT ATTTACTCTT CTCAAGGGTG TCATCAGTAT 1020
TCTCGGAAGG TCTCAAAAGT GGCAGGGTTC CACCTACCTC AGGTTTTTTT TGCATATTTA 1080
ATCTTTTATA TTTAATATTT AAAAACAATT TTTACATCTT TCACCGCAGG AATTTCCAGT 1140
TTGTAAATTG GAAAGCGCTG GAAAGCTGGA CCCACTCAGT AACAAGACAA CTCCAATCAA 1200
AGCAGGTGTT TGCAGGCATC AAGGTCAAGC TGGGCTGGGA CAGCCAAGGG CAGCCCAGAG 1260
GTCCTTCTCA TAGCACTACC TTCTCATAGT ACTACCCTGT CTTGAGCAAA GACCCTTGTG 1320
GGACCATCAG CAGGATTTGG ATGACTAACA GAGGGCAAAT TTCATGCTGC TTTGAGCCTA 1380
ATGCCTCTTT GTTTTTACTG CATTTTTTTT TAATTTTTTT TTTTTTATTA TACTTTAAGT 1440
TTTAGGGTAC ATGTGCACAT TGTGCAGGTT 1470
|
