| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18873 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:120158400-120159880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:120159217-120159238 | AGGGAGTTTCACTTTCTTATC | + | 6.07 | | LHX2 | MA0700.1 | chr4:120158905-120158915 | GTTAATTAGT | - | 6.02 | | Nfe2l2 | MA0150.2 | chr4:120158983-120158998 | TGCTGACTCACCTTG | - | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr4 | 120158622 | 120158685 | | chr4 | 120159259 | 120159657 | | chr4 | 120158800 | 120159822 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I119237 | chr4 | 120158894 | 120159628 |
|
Enhancer Sequence | GAATACAGTC AGTCTAGATT TATCATGATT TTTAAGGCCC TAGAATTTTC AGAATGGTAA 60
GTGAGCATTG GCTTCAACTT GAAGTCAACA ACTGCATTAT GTCCTAATAA GAGAGTCAGC 120
CTGTGGCCAG AAAGGTGGCC GCCCCCTCGC CCGTCACGCA ATGCATGTTC GTGGGGAACC 180
TGGTGCTAAA CTATTCATAG ATGACCTGCT TCTGGGTCGG GGTTTTGTAT GTAGCAGAGC 240
GGCTCCCTCG CTGCTATCTA TTGAAAGTCA GCCCTCGACA CAAGTGTTTG AAAAAATTAA 300
AAAATAATTA AAAAAAAAAA AGACAGAATC AGCCTGTCCT TTGAAGCTTT GAAGCCAGGC 360
ATTGACTTCT TTCTGACTGT GAATGTCCTA GATGGCATCT TCTTCCATCT GTCAATATCA 420
CTGTCAGTCT TCAACTGTTT CTTCCACAGA TGACAGTCTT CATCTGTCAA ACAGTTGATG 480
ACTGTTTCTT CAACACTGAA AATCTGTTAA TTAGTGTAGC CACTTTCATT AGTTATCTTA 540
GCTAGATTTC TGGATAATTT GCTGTAGCTT CTCCATCAGC ATTTGCTGAC TCACCTTGTA 600
TTTTTATGTT ATGGAGATGG CATCTTTCCT TAAACCTCCT GAATCAACCT CTGCTAGCTT 660
CCTACTTTTC TTTAGCTTCC TCACCCTCTT TTTCTCAGCT TTCGTAGAAT TAAAGAGCGT 720
TAGGGCCTTG CTCTGGATTG GGCTTTGGCT TAAAGGAATG TTGTAACTGG TTGGATCTTC 780
TATCCAGACC ACTCAAATTT TCTCACTATC AGCAATAAGG GAGTTTCACT TTCTTATCAT 840
TCAGGTGTTT ATTTGAGTAA CACTTTTAAT TTCCTTCAAG AGCTTTCCCT TTGCATTCAC 900
AACTTGGGTT ACTTACTGCT TGATGTAGGA AGCCTACCTT TCTGCCTGTC TCAACTTTCA 960
ACATGCCTTC CTCACCAAGC TTAGTCATTT CCAGCTTTTG ACTGAAAATG AGAGACATGC 1020
GACTCCTTTT ACTTGAACAC CTAGGGGCCA TTGTAGGGTT ATGAACTGAC GTCATTTCAG 1080
TACTGCTGCA TCTCAGGGAG TAGGGAGGCC TGAGGAAAAG AGAGAGTTGG GGAAACAGAT 1140
GGTCAGTGGA GCAGTCAGAA TACACACATT CATGGATTAT GCTTGCTATC GTATATGGGA 1200
GTGGTTCATA TTGCCTGAAA ACAATTACAA TGGAAACATC AAAGATAACT TATCACAGAT 1260
CAGCATAACA GATACAGTAA TAATGAAAAA GAATTACTGA AGTGTGACAT AGACATGAAG 1320
TGGGCATATG CTGTTGGGAA AATGGTGCTG GTAGATTGGC TTGCTACAGG GTTGACACAC 1380
ACCTTCAGTT TGTTAAAAAG GCAGTATATC TGCAAAGAGC GATAAAGTAA AATGCTATAA 1440
AACAAAGTAT TCTTGCATTT GTTTGTTTTT AATTCATAGG 1480
|
