Tag | Content |
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EnhancerAtlas ID | HS147-28400 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr3:57983300-57984120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr3:57983875-57983889 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23194 | chr3:57983235-57983553 | Colon_Crypt_1 | SE_27681 | chr3:57983550-57985724 | Fetal_Intestine | SE_28779 | chr3:57983357-57985641 | Fetal_Intestine_Large | SE_34631 | chr3:57983187-57987623 | HeLa | SE_36024 | chr3:57983983-57987598 | HMEC | SE_52474 | chr3:57983067-57983934 | Small_Intestine | SE_52474 | chr3:57983993-57985745 | Small_Intestine |
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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 |
GH03I057997 | chr3 | 57983265 | 57987431 |
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Enhancer Sequence | ATCACCTTAG GGGTCTTGTT AAACTGCAGC CCCTGATTCA GTGGGTCTGG GTGGCACCTG 60 AGATTCTGCA CACTCCCAGG TGACGTCCAG GCTGCTAGTG GGACCACATT TTTTTTTTTT 120 GAGACAGAGT CTTGCTCTGT CACCCAGGCT GGAGTACAGT GGTGCTATCT TGGCTCAGTG 180 CAACCTCTGC CCCAGATTCA AGCAATTCTC CTGTCTCAGC CTCCCGAACA GCTGGGATTA 240 CAGGCATCTG CCATCATGCT CAGCTAATTT TTGTATTTTT AGTAGAGGCG GGTTTCACCA 300 TGTTGGCCAG GCTGGTCTTG AGCTCCTGAC CTCAAGTGAT CCGCCTACCT CAGCCTCCCA 360 AAGTGCGGGG ATTACAGGTG TGAGTCACCT CGCCCGGCCC TAGTGGGACC ACATGTTATC 420 AGTCCACTAG TGAGGGATAT TTAGCTTGCT GTAAAAAGTG CTGCAATAAA CTTCCTTGAA 480 GATACATTCT GGAGTGCTAC AGAATAGGTT TTGGAGTTAG AAAGCAAAAG GGTGGCTGGG 540 CGTGGTGGCT CATGCCTATA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG 600 AGGCCAGGAG TTCCAGACAA GCCTGGCCAA CATGATGAAA CCCTGTCTCT ACTGAAAATA 660 CAAAAATTAG CCAGGTGTGA TGGTGGGTGC CTGTAATCCC AGCTACTTGG GAGGCTGAGG 720 CAGGATAATT GCTTGGACCT GCGAGGTGGA GGTTGCAGTG AGCCAAGATC GTACCACTGC 780 ACTCCAACCT GGGTGACAGA GACCCTGTCA ACAAAAAAAG 820
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