| Tag | Content |
|---|
EnhancerAtlas ID | HS190-11242 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr6:91060220-91061380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:91060581-91060599 | TCTTCCTCCCTCCCTCCC | - | 6.36 | | ZNF263 | MA0528.1 | chr6:91060569-91060590 | TCACTCTCTCTCTCTTCCTCC | - | 6.11 | | ZNF263 | MA0528.1 | chr6:91060576-91060597 | CTCTCTCTTCCTCCCTCCCTC | - | 6.5 | | ZNF263 | MA0528.1 | chr6:91060586-91060607 | CTCCCTCCCTCCCTCTCCTCT | - | 6.6 | | ZNF263 | MA0528.1 | chr6:91060580-91060601 | CTCTTCCTCCCTCCCTCCCTC | - | 6.71 | | ZNF263 | MA0528.1 | chr6:91060572-91060593 | CTCTCTCTCTCTTCCTCCCTC | - | 7.1 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_58370 | chr6:91058940-91135531 | Ly1 | | SE_59753 | chr6:91059505-91108225 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 91060788 | 91061282 | | chr6 | 91060521 | 91060684 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I090350 | chr6 | 91059902 | 91061387 |
|
Enhancer Sequence | GCTGTCTCTT CCACTAAGAT TGTAAGTTCC TTGAGGGCAG GGTCCTTGTC TTCTCAGTCT 60
TCCTAGCACC TTCTATAGTG TCTGGCACAG CAGTAAGAAC TCAATAAATA TTTGGGGAAT 120
AAATGTATCT GTATTTGCTT GAAATGGACA AGTGATATGG TTTGGCTCTG TGTCTCCAAC 180
CAAATGTCAT GTTGAATTGT GATTCCCAGT GTTGGAAGAG GGACCTGCTG GGAGGTGATT 240
GGATCATGGG GGCAGATTTC CCCCTTGTTG TTCTTGTGAT AGTGAGTGAG TTCTCATGAG 300
ATCTGTTGGT TTAAACACGT GTGGCACTTC CCTCTTTGTG CTCTCTCTCT CACTCTCTCT 360
CTCTTCCTCC CTCCCTCCCT CTCCTCTGCC ACCAGATGAC GACATACTTG CTTCCTCTTC 420
ACCCTTCTGC CGTAATTGTA AGTTTTTTGA GGCCTCCCAA CCATGCTTTA TGCTTTCTGT 480
ACAGCCTGAG GAACTGTGAG TCAATTAAAC CTCTTTCCTT CATAAATTAC CCAGCTCAGG 540
TAGTTCTTTA TAGCAGTGTG AGAACAGACT AATACAACAA GGTTCACGTA TTTTTCCTGT 600
AAGGCCCCCA AAGTTCTGCA TACATCAGTG GATGCAAATA GATGCTTTGA GGAGGAATAT 660
CACCATCTCC AGCTGTCAGG CTGATCGAGT CTGATTGGCA CCCACTAGGA TTTCCCTTAC 720
ACATGTAACA TGTGGGCTGC TGGAGGCAAA GGTAATGTTT AGTAGACCTC ATTCCTCATA 780
TCAGATCCAA CCTTCCTTGT CATCTCTTCT GACTGTCTTT CTGTTTCTGC TGGTTTGCTC 840
AGAGCCTGTC ACTGCAGCAC CTAATCAGGC CGATCTCTTT AGCACTGACC TAGTCTGGTG 900
TTGGACTTCT CTCCTTGTTA TCAAAACATA CCTCCCTCTT TCCTCAGTTC ATGAAGTTGG 960
AAGACACTTC TCTGCTACTG TGTGGTGATG GGGGCGTTAG TGGGGTAAAC AGTTTAACTG 1020
TTTTAACTTC ATTCGTGGTT AAGAGGTACC AGGGGCCCTC TGATAATAAA ACACAGCTAA 1080
GATGTATCTA AGGCTTATAG AAAGCAACAA TAAACCATTT TTGACTGTGC AGGAATTTAA 1140
GTTTTTATAT AAGAATATAC 1160
|
