| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00033 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:1608850-1611180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:1608900-1608921 | TGCTACTTTCTTTTTCCTTTT | + | 7.05 | | ZNF263 | MA0528.1 | chr1:1609881-1609902 | CTCTCTCTCCTCCCCTCCCCC | - | 6.93 | | ZNF263 | MA0528.1 | chr1:1609876-1609897 | CCTTCCTCTCTCTCCTCCCCT | - | 7.31 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_11139 | chr1:1605387-1611273 | CD20 | | SE_12366 | chr1:1608826-1610531 | CD3 | | SE_13835 | chr1:1608971-1610507 | CD34_Primary_RO01536 | | SE_14478 | chr1:1608779-1610803 | CD4_Memory_Primary_7pool | | SE_16023 | chr1:1608680-1610322 | CD4_Naive_Primary_7pool | | SE_16832 | chr1:1608885-1609698 | CD4_Naive_Primary_8pool | | SE_17401 | chr1:1606520-1611317 | CD4p_CD25-_CD45RAp_Naive | | SE_17899 | chr1:1606636-1611136 | CD4p_CD25-_CD45ROp_Memory | | SE_18811 | chr1:1608508-1610888 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19243 | chr1:1608825-1610748 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20145 | chr1:1606234-1610794 | CD56 | | SE_21296 | chr1:1608961-1609955 | CD8_Memory_7pool | | SE_22403 | chr1:1606348-1611102 | CD8_primiary | | SE_24735 | chr1:1609098-1611006 | Colon_Crypt_3 | | SE_27558 | chr1:1609143-1610981 | Esophagus | | SE_31250 | chr1:1609059-1611094 | Fetal_Thymus | | SE_32013 | chr1:1609095-1611198 | Gastric | | SE_41278 | chr1:1609070-1610751 | Left_Ventricle | | SE_50179 | chr1:1609063-1611140 | Sigmoid_Colon | | SE_52422 | chr1:1608577-1611296 | Small_Intestine | | SE_53355 | chr1:1608879-1610484 | Spleen | | SE_65325 | chr1:1609088-1611198 | Pancreatic_islets | | SE_69024 | chr1:1609052-1611070 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1609680 | 1610000 | | chr1 | 1609152 | 1610855 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001677 | chr1 | 1608732 | 1611112 |
|
Enhancer Sequence | TCTCGATGGG CTTTGTGGCT GCCGCTGTCG GGTGCCCAGG ACTAATTCCA TGCTACTTTC 60
TTTTTCCTTT TTTTTTTTTT TTTTGAGACG GAGTATTGCT CTGTCGCCCA GGCTGAAGTG 120
CAGAGGCGTG ATCTGGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCTCGCC ATTCTCCTGC 180
CTCAGGCTCC CGAGTAGCTG GGACGACAGG CGTCCGCCAC CACGTCCGGC TAATTTTTTG 240
TAATTTTTTT TTTTTTAGTA GAGACGGGTT TTCACCGTGT TAGCCAGGAT GGTCTCGATC 300
TCCTGACCTC GTGAACCGCC CACCTCGGCC TCCTAAAGTT CCATGCTACT TTCTAGACAG 360
ACTCCGTGGT ATAAAACCAC ACTTACACCC GCTTCACGCT CAGGCGACTG TGGCTTCGGG 420
GCGAGACACC CCCTCCCTTC CCACGAGCTC CAGGAAGGTC AGAACAGCCG TTTCCTCCTG 480
AGGTCCAGTG GGAATCATCC CCCCAGCTGG GGCTTTGCAC AGACGCCACT GTGACTCCGC 540
AGCACCGAGA CCCCACCTCC CCCAGGTCTC AATCCCAGCG CTCAGGCAGC CCGATTTCCT 600
GTTTCTCACA CCTGGGTTTC TCTTCCTGCT TCGGGGGAGG CTGTGCATCT GAAGGGGCGC 660
CCATCCTGTC TCACCAAGGC GCTCTGGGAG CGTGTGGTGC CGGCCGTGCT GCCCGACCCA 720
GTACCCCTCC TCGTCTCACT TCTCCCCCGG GAAACTGGGG TTCCCACCTC ATTCGTGACC 780
TCCTTCTGTG TTTATGTTTA TGCACTTGCG TGCGTGCCAT ATGTATACAT AAATATTCTG 840
TGTTCACACT GAGGGACGCA CGCCACCCCC TCCCCCATGA AGACCTCGCC TGGGTGCTCA 900
GGCCGGCCTC TCCCCCAGCT CACCTGCCCA GCAGTGCTCA GAGGTGCCTG AAACTTGGCC 960
TCCCCATACC CGGGAACAGG CGCTTCTGCC CTCTCCCCAG TGGCGGCAAT GCCAGGGCCT 1020
CTGCAGCCTT CCTCTCTCTC CTCCCCTCCC CCTGCTGTGT GTGTCTGTGC ACCCAGGTCT 1080
CCCCGTCTGC CCATCACACC GCCAGCTCAG TGCCACCCAG ACGCTCCCAG GCCACCCATG 1140
TGTGCCCTGA CCCCTCGGTG CACCAGGACA GCTGCCTCCA AGGGCACCCC AGGCCTCAGT 1200
GAGGAGAAGG CCGACCCCTC CACCAGTTCC CACAGCCTCG GAATAACAAA GGACTCATCC 1260
ACTCCTCGGG CCACTGACAG TGCCAGATCT CCACAAAGAC ACCATTCCCT TCTTCCTGTT 1320
CAGCAGCACA GTCCCACTGC TTAGCCTGGG GTGACAACAA GCTGGGAGCT AAACCTCCAT 1380
GGGCTGCAGC CTCCCTGGAG CTAGGACTGG CTGGGCCCTG AGCCAGGGAG CTAGGAGACT 1440
TTGTGCCAGT TTCCCGGACT GATGGGCCCT GGCTGGGGGT GGAGCAGCTA CCTGGCTTTC 1500
CTGAGGTGAA AATCCAACAA CAAAGGGTGC GGCAGAGCAA AAGGACAGAG CACTCGCGAC 1560
AGGGCTCCGC AAGGCAGGGG TGGAGCTCAT GGCAGGCGTG GATCTCACTC CCCACCTCAC 1620
TAGGCCTCAC GGCCCTTGAC CTCTCCCTCC CACCTCGAAG GCTGCCCCCT GGCTGGGGAC 1680
GCTGTCACAG CACCCGCTAC ACAGGCTCTG CCACCACCAG CGAGTTTCTA AAACCAAATT 1740
CATTTACATG GCAAGGAGGC CACGCTCAAG AAACCCCTCC AGGAGCAAGG AACAGCACGT 1800
GGGCTCGGGC GTGTGCAGAC GACGCCAGTC ACGTCCCACC TGACGTCGAG GCAAACCTGG 1860
AATTCAAAAG GCAAGCATCT CCCTCTTGCC AGAACAGTCT GTCCACTTAG CTTCCCTCTG 1920
AGAAACTCAC AGCATCCCAG GCAAAACTGC TCCCCGCAAT GAGGACCCCC ATTCCCCTTC 1980
TCTGCTGACA CTGTGCTCCA AGAAGCCTGT GGGACCCACA CAAGCAGCCC AGTCCCCACC 2040
CTAATGTTTG CTCACAATTA GTGGAAACAA AAAAACAGAA ATCACACTTC ACTGACGCTG 2100
CCGTTCTCTG TACATCAAGA ACTTAAGGTT CTGGGCCAGG CGCCGTGGCT CACACCTGGA 2160
ATCCCAGCAC TTTGGGAGGC CAAGGTGGGC GGATCACCTG AGCTCAGGAG TTCATGACCA 2220
GCCTGGCAAA CACAGCAAAA CCCCGTCTCT ACTAAAAGTA CAAAAAAAAA ATCAGCCGGG 2280
TGTGGTGGCT GGCACCTGTA ATCCCAGCTA CTCGGGAGGC TGAGGCAGGA 2330
|
