| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22686 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:50265840-50266810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr7:50266330-50266341 | TCAAGGTCAAA | + | 6.14 | | GATA2 | MA0036.3 | chr7:50266713-50266724 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr7:50266713-50266724 | TTCTTATCTCT | + | 6.32 | | Gata4 | MA0482.1 | chr7:50266714-50266725 | TCTTATCTCTT | + | 6.02 | | RORA | MA0071.1 | chr7:50266329-50266339 | ATCAAGGTCA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAACACCAAG GAGACAATAG AATATTGTGA CAGAGCTCAG GATCTGAAGT CCAACAGCCT 60
GGATGAGAAT CCCAGCACCA GTGCCTCCTA ACCACACACT CTTGAGCAAG ACCCTTCACT 120
TCCACGTGCT TCATTCATTT TCTTTATCTG TCAAGTGAGT TCATGACAAT ACATATCTCA 180
GAGTGTTACT ATGAGAATTA AAATACAGAG CACGTGTAAA GCATTTAGCA TAGTGCCTGC 240
AAATAGTAAT CTCTCAAAAA ACGTAAGCTG ATGCACTCCT TTACAAACAA AGAGTATCTC 300
TCTAAAACTC AGATTTCTAG GCACAGTCTC ATCAGTGTCA AAGCAATCAA AAAAACAAAC 360
AAAAAAGAGG TAGCATTCCA AGGTCCAAGG CTCTCAAAAG AAAGTGTGCT CAGAGGTTTG 420
GATAATGCTC AAACACGTAG CTTGGGTTTG AATTCTCAAA GAAAGTGCTT AAGATGAAAA 480
GGACATATAA TCAAGGTCAA AAATATGAGC AGATGCTTGA TGATTAGAAT GACACTTGTG 540
GAACTAATAC AGCGAAGATG GCTCCTCAGG CTGTGTTCCG AGCCAGAAAG GTGCAGACTG 600
GAGTGGCCCA GTGCTGGTGA TGGAAAGTGT GGGGAATCCC TGATAAAAGC AAAATGAAGC 660
CCAGGATGAG TGGGGAGGTA AGAGTTTCAG GCTGTGCTGA TTCATCTCAA GCCCAGTAAA 720
ATTACATCCC AGGCAACAGA GAAAATTTAC TAAGCTGACT TTTAATTGCT GTCAATATGG 780
TGCAGAGGCT TTAGATGCAG AGGGGCCCTG AGATCAAATT TCTGTTCTGC CGTCCTCTGT 840
TTCACTTCAG AAAGAATCAA ATTTGGGCTG ATTTTCTTAT CTCTTATCTT CTTAGCTCTG 900
TACATCCCAT CTGATTCATT TATATGATGA GAATGGTAGT ATTAGGTTGA AAAGTTTACA 960
ATAGCCAATA 970
|
