| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21598 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:109263230-109264540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr6:109264514-109264532 | GGTGTGGTTTCACTTTTC | - | 6.18 | | NFAT5 | MA0606.1 | chr6:109264382-109264392 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr6:109264382-109264392 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr6:109264382-109264392 | ATTTTCCATT | + | 6.02 |
|
| | 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 |
| GH06I108941 | chr6 | 109263143 | 109270434 |
|
Enhancer Sequence | CCAGAAATTC CCATAAGTCT TCATAAACAT TTCTTTAGTG GTTCTCCAAA TGGTTATCAT 60
TATGCAGCTG CCCTATCCAC TACTGCGAGT TCCTAAACAA CACAGACTTT GTCCTGATAG 120
ACCGAGATGA TGCTTGGCAA AGTAAGCTCA TAAGTGCTGG AAGAAAGAAT TTTGAGTGTG 180
TGAAATGCTT TGGCACCTGT AAGGTGTTAA AAAATATTTT TTCTAGTACT CGAGTGCTTC 240
TTCCTTAAAT ATGTACTTTC TTCTTCCTAG TTTGGAGGAA GAAATAATAA GAATTTTTTT 300
CCCACAATTT TCACATGGGT GGGCTGCCAT AAAAAGCAAA ACAGAATCCC TTCAGACCAG 360
CATGGCATCT TAGTTTCATG TTTCCCATGT CCCAGGTGGC CGATCAAATA TGATTTGTTT 420
TTCCTCTTAA TGTTCTGATG TGAGTGTATT GATCTGCAGT GGTTAGACAC TTTGCCGCAA 480
CTGGGATTTA CTTGAATGTT GAGGCTTGGA ACTGATTGTG GAGACCTGAA TCAGCCTTCC 540
AGCAACTTAT TTAAACAGAA TTATTACTTC CTATAATTAT TTTTTTTTTC AGCTCCTGGA 600
AACATCCCTG CAAGACTAAC TTGGGTTGTA GAGAAATACT CTGGAAGCTT TGTAGTCTCT 660
TAATATACAC AGCCATTGCC AAGTGATTAG ACAATCAGAA AGAGTCAGTA GACCTTCCCT 720
GTTTTTGTTC TGGGAGGTTA GTATTGCTTC TGTCTTGAAA GCCTGAGGAC TACATTTAGG 780
ATCAGCATAG GTTTCATTTT TCTAAGACAC ACTTTTAAAT CAAATCATGT TTATGGCTAA 840
TCGCGTTTTC AAAAAACATA GAAACAGAAA TCTAAAATGA ACAAGAAAGA AAAGAAAAAA 900
ACCCTTTATA GTGATAAATG AAATGTCACC TACACATGCC TCTTGAACTG ATCTTATCAG 960
CGGATGGGGA GCTTCACAGG AAGCTGCCGG TCGCTGCTGC CGTCCACAGA GGGGGAAATC 1020
CTGTTTTGAA CCAGGTAGCA CCAGGGCCGT TTGCTGTTGG AAGAAGTAGA ATATTTCCTC 1080
CCCATCTGCT GTTGTTTTCC ATTAAAGGGG ATAAAAATTA GAATTACATG AGAAGATACC 1140
AAAAGTCACA AAATTTTCCA TTATTTTTAC ATTCTTTTTC TCTTGTCAAG GTAAAGTCTG 1200
ATTTCAACAT ATGAGAAGTC TGAATATACT TTATATATTC GAGTATATAA AGTCTGAATC 1260
AAGTCCATCG ACAGGAGGGG TTGTGGTGTG GTTTCACTTT TCTATACAAC 1310
|
