| Tag | Content |
|---|
EnhancerAtlas ID | HS103-00652 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:56959070-56960410 |
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 | AGGAATGTCT ATAACTGTTA TTCTATGCCT GTTTCACCAG TGAATTTAGG GAGCAGATAA 60
CTTGTTTCTT AATTTTCACA GGTTCATAGA GAGCAATGTA TTCCAGGGTG GATTAAACAT 120
GGAGCCTCCT TTTTACCTAA TTTGAATGGG TTAGTTTAGA TGATGAGATT TGGGGTGTTT 180
AAGTTGTTAA GATTTAGGAT TTTGACTTGA TACTGCCATA TCCTAGGTCT TTAGGGGATG 240
TGGGGATAGG GTGATCTGTT TTGCATTTGG GATGGATGTG AATCTTTTGA GGGCCAGAGG 300
GTGAACTCTG GTACTCTGAA TAATGGTTCC CGAAATATGG CCATGTCTTA GATCCCTGGC 360
ATCTGTGAAT ATATGTTCCA TGGCAAAGAG GAATTAAGGC AGCAGATTGA ATTAAGTTTG 420
CCAGTGAACT GACTTTAATA TAGGTGATTA TCCTAGATTA TGAGCAGGTC TGTGTAATCA 480
GCAAGGAGGG CCTTTACATG TGAAAGGGGT GGCAGAAGAG GAGAACCAAA GAGATGGCAG 540
GGTGAGGACT CTACCCAATG TTGCTTCCTC CATGTGAACA TGAAGAGGGC CACAAGCCAG 600
GGAAAGTGGG TGGCCTCTAA AAACAGAAAA GGCAAGGAAA CAGCTTCTTG CCTAGAGCCT 660
CCAAGATTGT AAGACAATAC ATCTATGCTG TTTTACGTTT GTGGTAATTT GTTATAGCCG 720
CTATAGCAAA TTAATATAAG ACCTATCCTA CAATTTAATG CTCTAGGATC TTAGACTAAT 780
CATTTCATCT TTGCATTCTT TAGTATTCTT TCTTTCTCAA AATAACTGCT GTGAAGATCA 840
GACAGAACAA ATAGGCAGAA ATCCCTGGCA CACAGGTGCT CAATAAATGT GAATTTCTAG 900
CTTCCCCTTT TCTTCCAGGT TGGAGAAACA CAAGGAAGGG AAGCAGGAGC CACAGGCCAT 960
TCTCAGCCTT CCTTTGATGT GGGCTGTGTA CAGGATTCCC TCAGTAAGCT CCCCCAGCAT 1020
ACCTTATCTA GAGTGAGGGC TGCTTATCTG CCCTCGGGGT TCCTACAGCT CCTACCTCTC 1080
TGATGGAAAA ATCCTCTTTA GAATACAAAA GCTCTTTAGA AGAGCCTGAG ATGAGGGTAG 1140
AGCCAGGGCC TCATTCTGCA AACAGGCTTT CAGAGATGAA AGAGCAGGGC AGACATCGGT 1200
ATCTACCCTA TGACCACCAC ATTTCCCACT GAAAAAAATC AGGAGTTGGT GCGCTGAGAT 1260
GAGGCAAGCC CACTCAAAGA GGCCAGCCCG CGATGCTTCC TTCTCCTACC CACACACCTG 1320
AGACAAACAT CTCTCAAACA 1340
|
