EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS076-17436 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr14:50527570-50528340 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RELAMA0107.1chr14:50527884-50527894GGGAATTTCC+6.02
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_09329chr14:50526363-50533428CD14
SE_10501chr14:50526956-50533284CD19_Primary
SE_10886chr14:50526071-50535571CD20
SE_18721chr14:50525925-50533358CD4p_CD25-_Il17-_PMAstim_Th
SE_19344chr14:50526001-50533077CD4p_CD25-_Il17p_PMAstim_Th17
SE_20031chr14:50526652-50533273CD56
SE_22736chr14:50525921-50533251CD8_primiary
SE_26853chr14:50526389-50530026Esophagus
SE_28524chr14:50526852-50530302Fetal_Intestine
SE_33820chr14:50526831-50530087HCC1954
SE_50690chr14:50526375-50530034Sigmoid_Colon
SE_52900chr14:50526907-50530103Small_Intestine
SE_54444chr14:50526310-50530061Spleen
SE_58913chr14:50504199-50555614Ly3
SE_61107chr14:50504474-50555236HBL1
SE_62268chr14:50504167-50584388Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr145052761150528257
Number: 1             
IDChromosomeStartEnd
GH14I050059chr145052630150533240
Enhancer Sequence
TTCCCCATCC CCATCACTTC CTTGGGAGTC AGTGAAAGTC ACTGAGGTAA CACAGCAGAG 60
CGCTCGGCAT ATGAGAAGCG TGAGCCAAAT GTGAGCTGTT CTCTCCCAGG AGCGTGTCTG 120
AATGGGGCTG GAGATGGACG CCTCCTTTCC TCATTTCTCT CAGACCTCCT GGGGTGGTTT 180
CCTGTCACAG AACAGAAGCA ATTGCCTCAA ATCAGATACC CAAGGATGCT GCAGGGAGAA 240
GAGGCTGGAA GAGGGTGGCT GGGGTTTCAC TTGTGTAAGC CACACACCTA AAATAAGCCC 300
CCGCAGGAGA CTCTGGGAAT TTCCTGTAAT TTTCACTGTA AATGTCCTAT TTATAAAGCT 360
GAGTCACTGC AAGCCGTTGT TTCACAACCA CCCAGCATGT GGAGACAGGC CGGCACAGGA 420
AACAAGGAGC ATACCCCAAA ACGCAGGCCT CACTCATGGC CTTTGGGGGT TCCCTGGGGC 480
CAGCCTGGGC CTGGCCGTTC AGCCCCTGTA AACACCTCCA CAAACTCAGG ATTTGGGTCA 540
CTGGGCCAGG CTTACGCTCT CATCCCCCAT TAGCCCTTTT TCTGGCTTCT TTGCTCCAAA 600
ATAGTCTTTT TTTTTTTTTT TTTTTTTTTT TTGGTTATAC ATTTACAGGA AAAGTCTGGC 660
TTCTTCGAGA GTTGCTTACA GACAGTGCCA GGCCTGTCCC CTCTGGAGAC CTGAAGGGTC 720
TGGCCTTAAG TAGGATCCAG GGCAACTCTC TGCTTTCCCA CATGAATAGA 770