| Tag | Content |
|---|
EnhancerAtlas ID | HS030-01041 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:56959500-56960410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:56960038-56960052 | TTCCTTTGATGTGG | - | 6.12 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28999 | chr1:56959171-56960538 | Fetal_Intestine_Large | | SE_35745 | chr1:56958872-56963455 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I056493 | chr1 | 56959051 | 56963525 |
|
Enhancer Sequence | GACTTTAATA TAGGTGATTA TCCTAGATTA TGAGCAGGTC TGTGTAATCA GCAAGGAGGG 60
CCTTTACATG TGAAAGGGGT GGCAGAAGAG GAGAACCAAA GAGATGGCAG GGTGAGGACT 120
CTACCCAATG TTGCTTCCTC CATGTGAACA TGAAGAGGGC CACAAGCCAG GGAAAGTGGG 180
TGGCCTCTAA AAACAGAAAA GGCAAGGAAA CAGCTTCTTG CCTAGAGCCT CCAAGATTGT 240
AAGACAATAC ATCTATGCTG TTTTACGTTT GTGGTAATTT GTTATAGCCG CTATAGCAAA 300
TTAATATAAG ACCTATCCTA CAATTTAATG CTCTAGGATC TTAGACTAAT CATTTCATCT 360
TTGCATTCTT TAGTATTCTT TCTTTCTCAA AATAACTGCT GTGAAGATCA GACAGAACAA 420
ATAGGCAGAA ATCCCTGGCA CACAGGTGCT CAATAAATGT GAATTTCTAG CTTCCCCTTT 480
TCTTCCAGGT TGGAGAAACA CAAGGAAGGG AAGCAGGAGC CACAGGCCAT TCTCAGCCTT 540
CCTTTGATGT GGGCTGTGTA CAGGATTCCC TCAGTAAGCT CCCCCAGCAT ACCTTATCTA 600
GAGTGAGGGC TGCTTATCTG CCCTCGGGGT TCCTACAGCT CCTACCTCTC TGATGGAAAA 660
ATCCTCTTTA GAATACAAAA GCTCTTTAGA AGAGCCTGAG ATGAGGGTAG AGCCAGGGCC 720
TCATTCTGCA AACAGGCTTT CAGAGATGAA AGAGCAGGGC AGACATCGGT ATCTACCCTA 780
TGACCACCAC ATTTCCCACT GAAAAAAATC AGGAGTTGGT GCGCTGAGAT GAGGCAAGCC 840
CACTCAAAGA GGCCAGCCCG CGATGCTTCC TTCTCCTACC CACACACCTG AGACAAACAT 900
CTCTCAAACA 910
|
