| Tag | Content |
|---|
EnhancerAtlas ID | HS111-02755 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr19:49470140-49471380 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:49471144-49471165 | CTCTTCCCCTTCTCCTTCCCC | - | 6.08 | | ZNF263 | MA0528.1 | chr19:49471145-49471166 | TCTTCCCCTTCTCCTTCCCCT | - | 6.28 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_13994 | chr19:49464648-49471488 | CD34_Primary_RO01536 | | SE_28063 | chr19:49463660-49472037 | Fetal_Intestine | | SE_29249 | chr19:49463742-49472030 | Fetal_Intestine_Large | | SE_39950 | chr19:49463949-49471969 | K562 | | SE_50834 | chr19:49463688-49472130 | Sigmoid_Colon | | SE_52855 | chr19:49462932-49472076 | Small_Intestine | | SE_54141 | chr19:49464118-49472624 | Spleen | | SE_59464 | chr19:49464788-49471994 | Ly3 | | SE_65912 | chr19:49463924-49470362 | Pancreatic_islets |
|
Enhancer Sequence | GTGGTTTTGT GTGTGGTGTG GAAGATGAGG TGGGATCTGT TCTCATAAAG CTTCTGGCTG 60
GGTTGGGATG CCAGTGAAAG AGGAGTTGGC CCCATCTCCC ATTTTCTTAA CTGTCCTAAG 120
ACAAGAGGCT ATCTGGGTAG TGTTGAACCT GAGGGTTCTC TGCTTGCCTG GCTGTTAACT 180
GTCCCTCCCA GATGGTAGAG ATAGACTCCA GGGAGTTGAA TTAAGACCTA GGTTGGTATC 240
TAGAAACAGA TGTTAGGTCT CAGCCAGAAA CAGCCCTATT TAACGAGTGA TTATGGGGCC 300
AGGTGGGTCG CTCACCTGAT GTCAGGAGTT CGAGACCAGC CTGACCAACA TGAAGAAACC 360
CCGTCTCTAC TAAAATACAA AATTAGCTGG GTGTGGTGGC TCATACCTGT AATCCCAGCT 420
AGTCAGGAGG TTGAGGTAGG AGAATCGCTT GAATCTGGGA GGCGGAGGTT GCAGTGAGCT 480
GAGATGGCGT CATTGCACTC CAGCCTGGGC AAAAAGAGTG GAACTCCCAT CTCAAACAAA 540
AAACATGTCT GCCTCACGGA AGTTGCGGTG AGCTGAGATG GCGCCACTGT GCTCCAGCTT 600
GGGCAACAGA GTAAGACTCT GTCTCAAAAA AGAAAAAAGC CTCAATTCTG GGAGGCAGTT 660
GGAATTATTA GGCCCTTTAT ATGGGCACAT TGACGCTATT GCTATGCAAC TTGCATGGCA 720
ACCGGGGGGC TCACTGAGGT CTTTGCTCCA GAGTTTAAGA GATTATGGCC CGAGCTTGAG 780
TGATCCCAAT GTGAGGCGCA CACTGAGAGG AACTGGCCAG TGGAGCTGAG CAGCCAGGAA 840
CACGTGATGC CCAAGCAATG CTGGACAAGG GGTTTAGGGT TCATCACAGA AATGGGATGT 900
GAAACCTTGG GCCGGATTCT CCAAATGGGA ACTGAAGAAG CTTAAAACAG GCCTTAAAAA 960
GCACTTGCTG TGTCCAAGCT GCAAAACTGC TGTGTCAGCT CTGACTCTTC CCCTTCTCCT 1020
TCCCCTGGGT CTGGGGCAGG GTGGTTCAAG CCTGTAATCC CAGCACTTTG GGAGGCCAAG 1080
GCAGGACGAT CACTTGAGCC CAGGAGGTTG AGACCAGCCT AAGCAACATA GGGAGACCCC 1140
CCAAGTCTCT CTAGAATAAG AGGATGAGCT CAGACCAGGG AAGGGGTGGT ACTGGGGGGA 1200
CGTCACAGCC AGGCCCACCA AGTGTCATGT CTGACCACAC 1240
|
