| Tag | Content |
|---|
EnhancerAtlas ID | HS087-12075 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr2:85184820-85186880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr2:85185844-85185861 | GGGTACGTCCTGTACCT | - | 6.05 | | EWSR1-FLI1 | MA0149.1 | chr2:85184888-85184906 | GCTTCCTTCCTTCCTCTA | - | 6.04 | | EWSR1-FLI1 | MA0149.1 | chr2:85184880-85184898 | TCATCCCTGCTTCCTTCC | - | 6.06 | | EWSR1-FLI1 | MA0149.1 | chr2:85184884-85184902 | CCCTGCTTCCTTCCTTCC | - | 8.57 | | Foxd3 | MA0041.1 | chr2:85185139-85185151 | GAATGTTTTTTT | + | 6.52 | | JUN(var.2) | MA0489.1 | chr2:85186484-85186498 | ATGACTCATTACCT | - | 6.18 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_24195 | chr2:85185151-85185630 | Colon_Crypt_2 | | SE_25084 | chr2:85185063-85185733 | Colon_Crypt_3 | | SE_27502 | chr2:85184750-85187659 | Esophagus | | SE_32926 | chr2:85184713-85187023 | H1 | | SE_34685 | chr2:85184438-85187655 | HeLa | | SE_35873 | chr2:85183583-85187716 | HMEC | | SE_47378 | chr2:85183405-85188185 | Panc1 | | SE_52528 | chr2:85184768-85187231 | Small_Intestine | | SE_64856 | chr2:85184623-85187455 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I084956 | chr2 | 85183648 | 85188352 |
|
Enhancer Sequence | CGCCCGGCTG GGAATGTGAT TTATTAATAA GATCAATGAA TTAAAACATT GAAGTTGCTC 60
TCATCCCTGC TTCCTTCCTT CCTCTAAGCA TCCAGAGAGC CCTCTGATCC TTTGGGATCA 120
CAGACATGGG ATATTTTTAC TCTCCAGCAT GAACACATAG GTGGATTTAC TGTGAAACTA 180
CTGAAGCTTA CACTTCAGGG TCCCTGGCTT CCTCAAACAG GGCTTCCAAG CCCTATATCT 240
AATTTTGCAC TTCTTTCTTA AGAGTTGCCT GTACCAAATA TATAAGCCTC AGGGCCCCAA 300
ACCTGGATCC AGCCTGAGTG AATGTTTTTT TAGAGCCAGG TCTGATAGAA GCCTGTTTTT 360
AAGGAATTAC CAGGAACTGA GCATGCTGTT TTTGGCCCTC AGGGGTTTCT CTCAGAACTA 420
AGAATTTGGG GGCTGTCCTC AGTCACAGGT GCAGCCTGAA GTCTGTTCCC GCCATGTTCA 480
CTCTCCTCTA TTTACCATCA CCTGCCCCTG CTGCGTCTTC CTTTAAAATA CAGCCCTGGG 540
CCCTAAGCTT TGTGCTGATT CAAGCTCTTT GGAATTCAAG ACATCCAGGA ATCCGACGCT 600
CCAAGAATTT TCCCAACGAC CTCTCAGTGG GCCATTCAGG CAGGAAAGGA TACACACATT 660
CCTAATGGGG CCAGGGGCTG TGACTTAGCC TGTGTGTGGC TGAGAGCCTG CTGAATACAA 720
GGTGCTGGCA GTTGGCAGGG CTTCCCAGGG TGGGGACTTC TTGCTGAGCT CATCAGCAGG 780
CCCAGCTCTG TACCCATTTG TCCAGGGAAA AACCAACCCC TAATGGAACT GTTTGTTTTA 840
TACTCTCTCA TCGAAGTCAT AAATGACTCA CAACTAGAAT GTTATTAACG TGAGAACAGA 900
GGCCTACCTG GCAGAATAAT TGGTTTTGGT CATTTGCTCA GAGTGCCAGG CAAATCCACA 960
AAGCATATCA AATTACAGGT TAGAAACCTG ATGAATAAAC AAGAATAATA CTGTGAGTTC 1020
TCAAGGGTAC GTCCTGTACC TGTTTTGCCC ACTGTCATAT CTCCGGCAAG ACACAGTGAA 1080
TACAGCCCCT GACACATTGG AGGTAATCTA TAAAGAGTTA CTAAATGATT AAAGAAAAGG 1140
GATGAGCTGT TCTTAGTGGA AACACCCATT TCTCCTAAGA TGAATTCGCA TTCTTTTGGA 1200
CCAGTTCTTT CTAAATTAAC AGCACTACCC AGTGGTATCA GAGCATCTAT ACCTTTGGAT 1260
ATTACAACAA CTCTATAAAT TCTAATTGCT TCTTCTTTTT TTTTTTTTTT TTTGAGACAA 1320
GAGTTTTGCT TTTTCACCCA GGCTGGAATG AAGTGGCGCG ATCTTGGCTC ACTGCAACCT 1380
CCACCCCACC GGGTTCAGGC GATTCTCCTG CCTCAGTCTC CTGAATAGCT GGGATTATAG 1440
GCGTCCGCCA CCACGCTGGC TAATTTTTGT ATTTTCAGTA GAGACGGTGA AGCCATGTTG 1500
GCTAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCACC CACCTCAGCC TCCCAAAGAG 1560
CTAGGATTAC AGGCGTGAGC CACCGTGCCC AGCTGAGACG CTATAATTTC TAACCTATGG 1620
CTTCCCCTTT TCTGGATTCC ATGCAGTCCA CACACAAGCA TTCTATGACT CATTACCTCC 1680
TGAGCATCCA GCTTCTTAAC TGTTACATTC TAGGGATCTT TTCCACAGTA TGTTTCTAAC 1740
TCCTTGATGG TTTTTGGGGG AGACCTGGGT GACACACTTG GAACAGACCT GCTCCAGGGG 1800
CTTGTTACTT TGTGTGCATC CCGCTCCCTT CACTTTCAGG TGACCTCATT TTCTAATCTT 1860
CCTTAGAGCA ACCAATCCCC CATACACTGT CTCCTTCTTC AGAGAATCTT TCTATGTGGA 1920
TTTGTGCTTT TTAAATTGGC ATATGAGTTT TAGGCACAGT TGGACCAGGA AATGCCTTCC 1980
TGAGGAATTC AGCAGCTTCT AGAGATAAAA TGTGATAGAG CAAATTATGA GTCTGGGAAT 2040
CAGGACATCT GGGTTCCAGT 2060
|
