| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00541 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:27467710-27469540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr1:27468355-27468366 | GGGAGATAAGA | - | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23485 | chr1:27468927-27469377 | Colon_Crypt_1 | | SE_24258 | chr1:27468945-27469185 | Colon_Crypt_2 | | SE_31553 | chr1:27466490-27469439 | Gastric | | SE_42029 | chr1:27467720-27468908 | LNCaP | | SE_42029 | chr1:27468916-27469503 | LNCaP | | SE_52500 | chr1:27467946-27473366 | Small_Intestine | | SE_53642 | chr1:27468405-27470395 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 27467800 | 27468800 | | chr1 | 27468800 | 27469400 | | chr1 | 27467731 | 27468546 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I027140 | chr1 | 27466743 | 27473516 |
|
Enhancer Sequence | AAATTTTTTT AAAACAGGAT AAGTGACTTG CCCAAGGTCA CGGTGCTACA AAGTAGTAGA 60
GCTGAGATTT GAACCCAGGT CTGTCAAGCT GCAAAGCTTG TTTTTCTAAC CACCATGCCT 120
GTGGGCATGT TTCCAAAGGG AACTGCTCTG GGACATTCTT CTGCAATCCA GAGGTTCTGC 180
CCCAAGTAGA AGCTTCTGGC TGTGCCCAGT GAGATTTCAT TCAAGTATCT CATCTAAATC 240
CTACATATAC TTCAAGGCCT AGCTCAGTGG TCACTTGCAC AGCCTACTGG GATCTTCCCA 300
GGTACGAAAT TCTCTCTCCC ACCTCTAAAC TCCCGTAGAA TTCCATCTGC ACTTCAAATC 360
ACACCCCCTT TCTACTGTCT GACTGTTTTG CATCTGTACC GCATTTCTCA AACAAGTCGT 420
TGAGCTTGGT AAAAGAAGCA GTTCTCATGC ATCTCTGCAC CTTCCACCAG CCAGGCAGGC 480
AGTGCTCAGT CAGGGAAGCG GGTGGGGTAG GGTGCCTGCT CCCCTCCCCC ATCTTGCTGT 540
AACCTGAGTC TTAGGCTTTG CCCAGTTAGG TGAGTTGGCC CCGCCTCATG CTGGCATAAC 600
GCCTACCTGG TACAGCATCC AGATTCCTGT GGGTCCTGGC CACCGGGGAG ATAAGATCTT 660
ATTCCCTGGC TTGATGGCAA AGATGCTATA AAAAGCACAG CACCCAAGTT CAACATTGGC 720
TTGTGATGGA CTACACGACC TGAGGGATTC AATGGGTGAA GGCAGAAGCC TCTGGGCTGT 780
CTCAGAGGTC CCAAGACCTG TACTTGGCTC CCCTGTAAGG ACCAGTGTAA GGACCAATGG 840
TTTCTCTGCC AAGGACAGCT CCCTAATAGA TACCCCAGGA GGAAGCTGCC CTTCTTTAGG 900
CTTAAAGGGC CCACTGGAAG AACTGAGGTT TGCCAATGCT ACCAATATCC AAGCCAAAAA 960
CCACAGCCCC TCCTCTCGGT CCACTGTCCA GGTCTTACTG CCTAGGGACT CCTGAGTTAG 1020
TTAACAGAGC AGGGAAGAAG ACTGACTCTG CCATTAATTC ACGAGTGGCC TGGGGCCAAT 1080
CCTCTCTGGG CCTCAACTGG AAAAACAGAG AACTTGATCA AAACATCTCC ATTTCCCTTT 1140
GGGCCTGGGG GTTACAAGCT ATGATAAGGA TTTTTCCATC TCTAACATTC TAGAATTAGA 1200
ATATTCTATA CTTTCATTCC TAGAAGCAGA GTGAGAACAG AGAACAGGGA CCTTCAGTCC 1260
AGGAAACAGC AGAGGCCAGT CAGGGCTTCC TAGCTGCATC CTCAAAGCCT GTCCACCTTC 1320
AGAGGCTTTC TCTTGCGTCT GCTGCCTCAA AGGTGGTTGC TTCCCCACTA GCAGAGCCTC 1380
AGAGGTGTGC CTGGGCCCTA GCCGCTTTAG GGAAATGGGC AGGTGGCCTG AGTCACCTAC 1440
TGTGTGTGAG CTGGGCTCAC CATGGCAACC CAGCAGACCC AGAGGGCATA AAGAAGCCAG 1500
TACCTTCCCT GCTGCACAGT GTAGGCGGAG CATGTTGCAT CTGCTTTGAT TTCCAACTTA 1560
GAAAAGTTTT TCTCTACTTT AAGGACTCAT TTCCCCTTCC CTTCTCTCAG GACACAGCTT 1620
ACTCACTCTG GGGTCCTTCT CCTTGCCTGG AAGGTATTCT GCAGTCCCAC AGGCAAACCC 1680
CACTCATCCC AGAATTAAGT ACCACCTCCT CCAAGGATTC ATCCCAGACC AGTTAGTCCT 1740
CTACCCTTCT TCAAGTTCCC ACCACACAAA AGGCAGAAGC TCTTAACCTT CAGAATCTGT 1800
GGCTTACACA CTGACAATCA ACTGTGTAAA 1830
|
