| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01240 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:111731870-111734760 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:111732142-111732153 | AAATCACAGCC | + | 6.02 | | TCF7L2 | MA0523.1 | chr1:111733055-111733069 | TTTCTTTGATCTTC | - | 6.64 | | Zfx | MA0146.2 | chr1:111732546-111732560 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_00548 | chr1:111731103-111739856 | Adipose_Nuclei | | SE_09820 | chr1:111732766-111737633 | CD14 | | SE_11520 | chr1:111707642-111752738 | CD20 | | SE_11981 | chr1:111734412-111740334 | CD3 | | SE_14851 | chr1:111732908-111748239 | CD4_Memory_Primary_7pool | | SE_17406 | chr1:111727560-111749237 | CD4p_CD25-_CD45RAp_Naive | | SE_17935 | chr1:111728556-111748584 | CD4p_CD25-_CD45ROp_Memory | | SE_18363 | chr1:111727276-111748673 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19522 | chr1:111734154-111744848 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20205 | chr1:111729924-111733846 | CD56 | | SE_22036 | chr1:111730652-111732723 | CD8_Naive_8pool | | SE_22036 | chr1:111733937-111748137 | CD8_Naive_8pool | | SE_22415 | chr1:111727440-111732571 | CD8_primiary | | SE_22415 | chr1:111732656-111748767 | CD8_primiary | | SE_25351 | chr1:111729155-111732373 | DND41 | | SE_25351 | chr1:111732691-111754239 | DND41 | | SE_27328 | chr1:111734461-111737751 | Esophagus | | SE_32304 | chr1:111734292-111735250 | Gastric | | SE_32464 | chr1:111734374-111749255 | GM12878 | | SE_50246 | chr1:111732689-111748417 | Sigmoid_Colon | | SE_52868 | chr1:111732755-111744865 | Small_Intestine | | SE_53613 | chr1:111731924-111739395 | Spleen | | SE_62234 | chr1:111732684-111775273 | Tonsil |
|
| | 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 |
| GH01I111181 | chr1 | 111723957 | 111732373 |
|
Enhancer Sequence | AGGACCTGAA ATAAACATAG ACTGGCTTTC TCTGGTCCTC TTTCTTCATA GACCCCCAGA 60
GGATTTACCG TCTTGATTTC TGCCTGTGGC TGTATCTTTC AGCCCAGGTA GCAACAAAAT 120
CAATATCTTC AGTTCTCATT TCCTATCTAG CATTCTCCTT TCTCACCATT CCCCTCTGGA 180
GATCTCAGTT CCATTCCTGA GGAAAGGGTG TGGGTGTTTG TAGGAAGGGA GTAGGAGAAA 240
GAGCTAAGGT AGAAGGGAAA TACAAGATGG AGAAATCACA GCCAGTCACT CCCTTAATAA 300
AACATTGACT GCAGAAATTG CTTCTACATG GAGCATTTAG TACATTGTTC ACATAAGTGC 360
TTTACACGTT TGATCTCAAG CAACAGTCCC GTGAGGCAGA TACAATCTCC ATTTTGAAGA 420
TGAGGAAACA GACCCAAAGA AGCTGCCCGA GGTCATACTA TGCTGCTAAT AAGAGAACCA 480
ATTTTTTTCC AAGCCTAGAC TGATATTCTT GAGATTGCAT TCCTCTCTCT ACAATTCCCC 540
TTCAACTCCC TGCTCTCTAG AACAGAGACC AACATCTTTT TATTTTTTTC ATGCTTGCAA 600
CATCTTATGT ACAATTTTCT ATTAGAAAAA CTCCTGCCTC TCGTGGTGGC TCACGCCTGT 660
AATCCCAGCA CTTTGGGAGG CCGAGGCGGG TGGATCACGA GGTCAGGAGA TCGAGACCAT 720
CCTGGCTAAC ACGGTGAAAC CCTGTCTCTA CTAAAAACGC AAAAAATCAG CCGGGTGTGG 780
TGGCGGGCGC CTGTAGTCCC AGCTACTCCA GAGGCTGAGG CAGGAGAATG GCGTGAACCC 840
GGGAGGCGGA GCTTGCGGTG AGCCGAGATC GCGCCACTGC ACTCCAGCCT GGGCGACACA 900
GCGAGACTCT GTCTCAAAAA AAAAAAAAAA AAAAACTACC TCACAGCTTT GGGCCTTCCA 960
GCAGGAAACA GCAAAGGAAG AAAATGAGCC CAGGGTCAAC AGGAAGAGGA AAGGAAAGGA 1020
AGTGAGGAGA CCATGTGTCT ACAGTCCTCA AGTGAGATAA GCACTGGGCT GGAACTTGGG 1080
GGACCTGAGT TTTAGCACTG GCCCCATCAC TGCCCAGGGA GCCTTCAGTC TAGACCAGAG 1140
ATTACAAATA GGCATCCTGC TGGCTGATTC CAACCAGCAG ATCTGTTTCT TTGATCTTCA 1200
CAGTATTTTT AAGTAATTGA TTTGGTTTCC AATATTTAAA CTGGACTATC TCACATAAAG 1260
TTTGGATTTG GGGCTTCTCC TGAAAAGTCA GGAGATCTAA CACTGGGTCC ACATTTCTAA 1320
AGGACAACAC TCAGATGGAA CTGAGTAGCA GTTGCCTGCT TTAGGCAGGG CATGTTCCCA 1380
CCAGTTTACC GTAACTTCCC AAATCATGTA TTGGTCATTT AAATGCCCGC TGGGCCTCTC 1440
TTTTCCATTT GTGACCCTTG GTCTTGATAG AGAGAATGAT CCCTCCATTG TCCCTTCTTC 1500
CAAATACAAG GAGAGAGTGG AAAGTATGCC AAAAAATAGA GCATGCACTG TAATTATCTG 1560
TCATCAGGGG AGAAAAGTTG AACTAGTCCA GGCCTGAAAC CACTTGTATA CATAGGCTCA 1620
GATGCCTTCA TGAAGGGAAG ACTGTTCCTT TGAGGGATTG GGGGGAGAGA GTGTGTATAA 1680
ATAATTTGTT TTTCAAGATT GTTCCCAGAA ATCTTTCCAG TATTTGGGCA TATTATTGTC 1740
TGTGGAGTAA TCCCTTACCA AAAGCCAGAG TCTGACTGGC CATCAGGAGA GGAGCCACGG 1800
CTTCCAGGGA GCTGGAGCTG CAGAGTCAAG AAGTTTCATA ATTTCTGGGG TTGGAACATT 1860
TAAATGTTTA TTGCTAAACA TGGGGCTAAT ACTCTGTCCC AGTTAGTCAC AAGGCTAAAG 1920
CTGGTTCAAA GGGCATGTGT ACTCAGCAGT CCTAAGGAAG GATGAGGGGG CCGGTGGAGC 1980
AAAGAAGGGA AACACAGCCT TCTTCTTTAC TTTGCAGCAA TGGTTTCTAT AGGAGAGGAT 2040
TTGGTTTTAT CTGTGCTAGG TTCCACTGTT GTCTATGTGG CCTTGGATAA GTCTCTGGAG 2100
CTCAGTTATC TCTTGGAGTG AGTCAATGGT TATGGCCAGG GCAGACATTC CCAAGTCCCT 2160
CTTCTGGCTT GAGATACAGT AACATACTAT CTTTTGAAAG TCCCTATACT GACAACTCTA 2220
AAGCACATGT TTTGAGTTAT TTTTCCAACA GCGGGGATAG ATTTACGCTT TTAATGCCCA 2280
TTTTCACAAC TGAGTTCTCT GGTGTGTCTG GTGCACTGCC AAGATGTAAG AAGCTAACAA 2340
AATCAAAGAG GATTCAGACC TATATCCTCA TTAGCCACCT TAGCTCTGAG CTACTCAGAA 2400
AGATGACTTG CTGCAAAAAT CTGCATTTTT AAGACTCATA GTTTGCCAGA GGGCCATGTT 2460
AGCTCAATTC CAAGGAATTC AAATACATTC CAGTGGGGTG TGTGTTGTAT AGACCAGCTG 2520
TGTCATACAT TTGGATGAGA TGGGACACCC CGAAGACTGC TCATTAGGGC CAGCTGGCAC 2580
AGAACAGTCT GCTCACCCCT GAATAAGCTA TCCACTGCCC CTTATGCCTA AAGGGGAATC 2640
CTTCAGAAGG GAACCTGCAT TTATTGAGCA TCACCTGTGT GTCGGGTGCC AGGTTAGGAG 2700
CTCTAGGCAG GTGGTTTCCC CCAGAATCCT TAGGAAGTGA ACACTGTTAT CCCCATTTTA 2760
GAGATGAGAA AGCTCAGGCT TAAAGAGGTA AGGTAACTTG CCCCTAATCA CACAGCTGTA 2820
AGCAGCAGAG CTGGGATCTG AATCCCACTC TACCTGGCTC CAAATCATGC ACTCTTCTTG 2880
CCACATCATA 2890
|
