Tag | Content |
---|
EnhancerAtlas ID | HS048-10138 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr13:28022470-28024200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr13:28024163-28024174 | TGCGCAGGCGC | - | 6.62 | Nr2f6(var.2) | MA0728.1 | chr13:28022959-28022974 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr13:28022959-28022977 | GAGGTCAGAAGTTCAAGA | + | 6.88 | Twist2 | MA0633.1 | chr13:28022828-28022838 | ACCATATGTT | + | 6.02 |
|
| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_10692 | chr13:28019321-28026509 | CD19_Primary | SE_11680 | chr13:28018577-28026786 | CD20 | SE_12042 | chr13:28023002-28026410 | CD3 | SE_13592 | chr13:28018257-28026305 | CD34_Primary_RO01536 | SE_14668 | chr13:28022851-28026461 | CD4_Memory_Primary_7pool | SE_17560 | chr13:28019266-28026656 | CD4p_CD25-_CD45RAp_Naive | SE_17995 | chr13:28022578-28026759 | CD4p_CD25-_CD45ROp_Memory | SE_18655 | chr13:28022360-28026861 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19517 | chr13:28022778-28026101 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20353 | chr13:28022299-28026271 | CD56 | SE_22112 | chr13:28022763-28026498 | CD8_Naive_8pool | SE_22591 | chr13:28020301-28026425 | CD8_primiary | SE_25456 | chr13:28018398-28026664 | DND41 | SE_28157 | chr13:28022353-28026510 | Fetal_Intestine | SE_29360 | chr13:28022294-28026486 | Fetal_Intestine_Large | SE_30768 | chr13:28022285-28025833 | Fetal_Muscle | SE_30949 | chr13:28019452-28026471 | Fetal_Thymus | SE_53141 | chr13:28023048-28026293 | Small_Intestine | SE_54432 | chr13:28022431-28022914 | Spleen | SE_54432 | chr13:28023096-28026018 | Spleen | SE_55388 | chr13:28022391-28022777 | Thymus | SE_55388 | chr13:28023207-28025910 | Thymus | SE_59291 | chr13:28019745-28030833 | Ly3 | SE_66707 | chr13:28020400-28022994 | Jurkat | SE_66707 | chr13:28023137-28024329 | Jurkat |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTAAATATT TGTGAAATTA ATTTTGCCAA TTCTCATGAC TCTAAGAACT CTTTTACACC 60 TTCCAAAGAA GTTTCATAAA GTCCTTGCTT CTGCCTGCAA ACTGTCCCAG TTGCCCCATT 120 CTGGCCTGAG CAGTGCAGCC TTAATCCCAG AGGGCCTGCG CTACCGTTAC TGGGCCTTCA 180 TGCTCCCCTC CCTTGGCTCT GGTTTTGCTC TTCCATAGGG AGCACAAAGT GTACTCTCCA 240 TAATGAGGCT GAGCTGTTTA CGTGCTAGAA CTCCCATTTA GAACACTGGA AAAAGCCAAC 300 ATTATATCTT TGGCCAACTA TTTAACCTTA TTTCTTTAGC TATTAAATTG AAATAATAAC 360 CATATGTTTT AAAAAGCTTT TAAACCCAGA GCTAAAGACT CTGTATTAAA AACTGGACTT 420 ACGGCCGGGC ACGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGGAGGC TGAGGAAGGC 480 AGATCACTTG AGGTCAGAAG TTCAAGACCA GCCTGGCCGA CATGGTGAAA CCCCATCTCT 540 ACTAAAAATA CAAAAAAACT AGCCGGGCCT GGTGGCGTGA GCCTGTATTC CCAGCTACTT 600 GGGAGGCTGA GGCAGGAGAA TCACTTGAAC CCGGGAAGCA GAGGTTGCAA TGAGCTGAGA 660 TCGTGCACCG CACTCCAGCC TAAGCATCCA GCCTAGGCAA CAGGGTGAGA CTCTCAAAAA 720 AAATTTTTTT TTAACTTATT CTCCTATGTT AATCCTATGT TAGTCTTCTT CCAGAACTCT 780 AGTGATGGGA TCACTACCCA TCCACAACCT CCAGTCACCT CCAAGACACC TTTGACGCCT 840 CCACTTTCCC AGTCAACCCA ACACCAAGCC TCATCGACTT CATTTCCTAA ACCCCACTCG 900 AATCCATCCA GTCCTCTCCG TATCCACTGT CACCACCGTC AGTTTAAAAC ATCGACCACC 960 TCGTTTGGAT TCCTGCCAGT CTCCTAACTC GGCTTGAGCC CTGGCAACCA GTTCCCACTG 1020 CACTGCGGTC ACTACACCCA GGACCTTCCT CACCTTAAAT AAAACTGCCC CGAGATTAAA 1080 GATCTACACC TTCGCCAGGC CAAAAGGCCC TTCCCACCTC TCCAGTTTCT TCTTTATGCC 1140 TAGGCCACAC TGGCCATTCG GTTTTTGAAA TACAGTACTC TCGTCCTTGG TTTAGGAAAC 1200 GCCAGATCCT TAGCGCATTC TTCTGATTAC CTTCCAAACT AAGCCAGTTC TCCCATCCCT 1260 CCCCCAATTT ACTGAGCTTA ACACTGAATG CTTCTACAGT CCAGTTGACC TTTCCTTTAA 1320 AACATTCATT ACAATTACAG TTTTGTGATG ATCTTAGCAC TGCTGTTCTC CATCACTAGA 1380 CCGTAAACTC TACGAAGCAG GAACAAAATG GACTTATTCG TTACTGTGTT GTGCCTGACA 1440 GAATGAATAG TAGTCGATTT TCAGATTCTT CTCTCCATCC TCTACTTTTC TAAGACTTAG 1500 GCCTTTCACA ACACGTACTT GAAACTGAGA CTTCTCAGTA AGAGAACTTC GTTTACTTGG 1560 TTCAAGTCTT AAGCCACGGA GCCCACTAAA TGACAAATGA GAAAAAAAAT CCCAGTCACT 1620 TCGCGACCTT CCCCCATAAG GCCTCCTCCC GCAACAGCAG GCAGCAAGAA CAACGCATTT 1680 GTCCAGCATG TCCTGCGCAG GCGCCCTTCG CCTGGCTCGC TCTGCCCCAC 1730
|