Tag | Content |
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EnhancerAtlas ID | HS048-02411 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:154915900-154916550 |
Target genes | Number: 35 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:154916423-154916442 | GGGTGCCACCTAGTGGTTC | - | 6.5 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_10773 | chr1:154914194-154917610 | CD19_Primary | SE_11976 | chr1:154914181-154916693 | CD3 | SE_12908 | chr1:154916071-154916702 | CD34_Primary_RO01480 | SE_16355 | chr1:154914534-154916090 | CD4_Naive_Primary_8pool | SE_16929 | chr1:154913661-154916990 | CD4p_CD225int_CD127p_Tmem | SE_20883 | chr1:154915952-154917646 | CD8_Memory_7pool | SE_22356 | chr1:154914220-154917138 | CD8_primiary | SE_27195 | chr1:154915760-154917372 | Esophagus | SE_28280 | chr1:154915844-154918584 | Fetal_Intestine | SE_29277 | chr1:154915792-154918273 | Fetal_Intestine_Large | SE_43530 | chr1:154907507-154922645 | MM1S | SE_52835 | chr1:154915811-154918586 | Small_Intestine | SE_53787 | chr1:154912441-154917339 | Spleen | SE_59728 | chr1:154908004-154930021 | Ly4 | SE_62808 | chr1:154907953-154929742 | Tonsil | SE_67174 | chr1:154907507-154922645 | MM1S |
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| 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 |
GH01I154940 | chr1 | 154912477 | 154918501 |
|
Enhancer Sequence | GCCACGACAC CCGACCCAAC TTTAGGCTTC TTAAGGTGCC TCTGTATTCC CAGTGCCTCT 60 CTGTTTCTGG TACACAGTAG ACTTTATAAA TGTTTGCTGA ATTAGTGGTC CTTGTTCCAT 120 CCCCAGCCTG CCCTAACCCC TGCCCCACCC ACACATGAAT TCAATGAACT AATACCTTTA 180 AGCCCTTAAA CAGAGTTACA TATTCGCTTG CTAAATAATA CAGAAATCAG TTACAGCCCC 240 TTCTAGAACC TGTAGTCCCC CGCCTCCTGC CTGAGCAGTC ACACCACATT ATTCTGTCTC 300 CTGTACTTCC TGGGCATTTC CAGGGTCATC AAAAAGCCCA GTGTATTGCC GAAGGGACTA 360 AGGTTAGATC TCAGGAAGGA CTTCCTAGAG AATAGCCAAG GGGAGTCTGG TCATCCTGGG 420 AGAGCTGGCC AGTGGAGCAG GCGCTGGGGT CAGTGGGGTA GGGTCTGAGA TTTTGGGGAC 480 AGTGAGTAGT GGGAGAGGCG AGGTCTGGAG CAAAATGGAG CCAGGGTGCC ACCTAGTGGT 540 TCCCTCACCT CCCCAGCCCC AGAAGCTCTT CCTTCTGGGC CTGGGTTCTT TTCCCTCCTC 600 CACACCCTTC CCTAAAGAAG GCAATAACTT TTGAGTGCCC AAAACAGGAG 650
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