| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18962 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:140898830-140901100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | - | 6.41 | | Ar | MA0007.3 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | + | 6.6 | | NR3C1 | MA0113.3 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | - | 6.53 | | NR3C1 | MA0113.3 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | + | 6.59 | | NR3C2 | MA0727.1 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | - | 6.52 | | NR3C2 | MA0727.1 | chr4:140900848-140900865 | GAGGACACAGTGTTCCT | + | 6.79 |
|
| | 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 |
| GH04I139975 | chr4 | 140896156 | 140900914 |
|
Enhancer Sequence | AGCCCAGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATCA GCTGGGTGTG 60
GTGGCATGTG CCTGTAATCC AAGCTACTCA GGAGGCTGAG GCAGGAGAAT TGCTGGAACC 120
CAGGAGGCAG ATGCTGCAGT GAGCCAAGAT CTTGCCACTG CACTCCAGCC AGGGCCACAG 180
AGTGAAACTC CCTAACAAAA AAACAAAAAA CAAAAAACAA AAAAAAAACA AAAAAAGGAT 240
CTTCTATGCT CTTTTCTGTT CCTACACAGA AATTACAGGA AATTCATCAC AGAATCAGTG 300
AACACCAAAG CTGAAAGGGA CTGCAGAAGG TAGCACAATG GATCCTCTCA CTTTACTGAT 360
GGGAGGGGAA GTGGTGCAGA CTGAGGTCAC AGTCTTGCTT TCAGGCCCCA GCTGGTCAGT 420
TTCAGAGCTT GGATTAGAAT TCACTCCATC CCTCAGGTCT GTGCTCCTTC TCCTTGACTC 480
GGAAGCAAAT GTGAAGAATG GAGCCCAAGA AGGTTACAAA AAAAAGTCTT TGGACCAAAG 540
TCTCTCTCTT GATTTCAGCC TCAAAGGAAG TGAGCTAATG TGGAGATGCA TGGCACTCCT 600
GGCTCCCCAT CTTTGGGAGT GGTGAGCCTC CCAAGCACAG GAAGATTCAG CACCAACTCT 660
AGCTGCAGAT CTATCCCAAG GCCCAGATTG CATTAGCCAA GACCTCTCCA GGAAGCCTGT 720
TGGAGTGAGC AGAGAAGAGC CTCAACAGGT GGCAAGTGGT CTCAAGTGCC ACTTCTCTCT 780
GAAAGGAAAG TCCTGCAAAA ATGAAAATCT GCAAATGCTT TAAAAACGAG TGGCAGAGGA 840
TGGCGTCTCT GCCCTTTCTC CTCCTGGGTA AAGGGCAGTT GACCCTCACT ATGTCTTCCA 900
AATGCCTCCC ATGACTTCCC AGCATCAACC ACATCAAAAA AAAAGAGAGA GAGAGAGAGC 960
ACACAACTGC GCTAGGCATT CACAACATTC TCTTCCTTCA GGGGCTCCAA TCTGGGCCCT 1020
GGCAGGTTAT CAAAGAGACT TGGGTCTCTT TGTCCCCCAT CCCTAATCTG TCTTGGTGTC 1080
TCTCTTTGGC CCTCCCATGG ATGACATCCC CCCCAGAGAC CTTGCCAGTC AGCCTGCCCA 1140
CCTGGCCTCC CCACAGAACT GGCTATATAG CAGGAAACGG ATTTGCCACT TCTCCATTTC 1200
CAGATGGCAC TGAAACAAGT ACACATCCTC CTTTCACTTT CAAAGAGCTC TATGACTACT 1260
TTCAAAGAGC TCTATGACTA CTTTCAAAGA GCTCTATGAC TAGTTACCTT AGAGAAACTG 1320
ACAGAACAAA GGAACAAGCC TGCTTATGTG GTACTAGTAA AATCATAATA TCAGCCACTA 1380
CTTATGAAGC ATTTTGTATG TGTCCGGCTC TGTATTAGGT GTTACACCTG CATTATCTAC 1440
AAGCCTTTCA TCAATCCTGC AAGGAAAGTA TTAGTTTTAC TCCCATTGTA AAGGTGAGAG 1500
AACTAAGGAT TAGAATGATT TGAGACCACA GAACTTGTAA ATAAAATTTT AAACATTTTG 1560
GTCTAAGTTG CCTTTCTCTT CAACATGCTA GAAATGAGTC TAGACTTACC TGGCTCATAG 1620
CTCCCTCTTT AGCTCTTTTA CATGGCATTC ATTTAAACAT GCCTTCTCAC ATTTTTCTGC 1680
TTGGAGGCAG AGCTTGTCCA ACCACCCCTC CATAGACACC ACTGCCTCCC AGCTCCATTT 1740
GCCCCTGTCT GCTGAGCTCC TTCTATACTG TCCACATGTG TTCTCTAGTT GCTGCTTTAG 1800
CTCTATCCAT GCCCAGCCAC TAACAGTTGG GTTAGTGGTT GCTACGGTTT GAATGTGTCC 1860
CCTCAAAACT TCAGGTGTTG CCAATGTGAC AGTATCAAGA GGTAACAGGG CCTTTAAGAG 1920
GCCATGAAGG CTACTCCCTC ATGAATAGCA GTAAGGCCCT TATAAAAGAG GCTTCCCACA 1980
GTGTTCAGTT AGCTTGATCT TCTACCTTTC TGCCATGTGA GGACACAGTG TTCCTCCCCT 2040
TTAGAAGATG TGGCATCAAG GTACCATCTT GGAGACAGAG AGTAGCCCTC CCCAGACATC 2100
TGAACCTGCT GGTGCCGTGA TCTCGGACTT CCCAGCCTCT AGAACTGTGA GAAAACAAAT 2160
TTCTGTTCTT GATAAATTAC CCAGTCCTGG GTATGTTGTT ACAGCAGCAC AAAATGGACT 2220
AAGGCAGTGG TTCTCTGGAA CAACTGCCAA TAGTAAGTAG GAATATCCCA 2270
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