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

TagContent
EnhancerAtlas ID
HS060-32864 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr7:158607280-158608390 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr7:158608113-158608131TCTATCTTCCTTCCTCCC-6.09
Sox3MA0514.1chr7:158607731-158607741AAAACAAAGG-6.02
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00536chr7:158607035-158615368Adipose_Nuclei
SE_09720chr7:158607058-158615231CD14
SE_12133chr7:158607115-158608837CD3
SE_13427chr7:158607137-158608236CD34_Primary_RO01536
SE_13427chr7:158608256-158619135CD34_Primary_RO01536
SE_14407chr7:158607012-158615260CD4_Memory_Primary_7pool
SE_15895chr7:158607095-158608288CD4_Naive_Primary_7pool
SE_17029chr7:158607265-158608996CD4p_CD225int_CD127p_Tmem
SE_17509chr7:158606909-158615488CD4p_CD25-_CD45RAp_Naive
SE_18013chr7:158607080-158615412CD4p_CD25-_CD45ROp_Memory
SE_18652chr7:158607144-158615340CD4p_CD25-_Il17-_PMAstim_Th
SE_19390chr7:158607158-158615370CD4p_CD25-_Il17p_PMAstim_Th17
SE_20308chr7:158607068-158613047CD56
SE_21549chr7:158607008-158608781CD8_Naive_7pool
SE_22210chr7:158606982-158608780CD8_Naive_8pool
SE_22705chr7:158607034-158615344CD8_primiary
SE_26128chr7:158607049-158615347Duodenum_Smooth_Muscle
SE_26837chr7:158607149-158609583Esophagus
SE_30423chr7:158607172-158612328Fetal_Muscle
SE_37489chr7:158607138-158615462HSMMtube
SE_39789chr7:158607078-158608910Jurkat
SE_41194chr7:158607181-158610523Left_Ventricle
SE_42532chr7:158607170-158612056Lung
SE_46345chr7:158607115-158615237Osteoblasts
SE_50581chr7:158607114-158609511Sigmoid_Colon
SE_52760chr7:158607174-158609504Small_Intestine
SE_54172chr7:158607756-158608274Spleen
SE_55042chr7:158607039-158615094Stomach_Smooth_Muscle
SE_62817chr7:158601938-158623708Tonsil
SE_66523chr7:158607078-158608910Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7158607400158608000
Number: 1             
IDChromosomeStartEnd
GH07I158809chr7158602158158618736
Enhancer Sequence
GAATGCTAAC AGTATATAAA CTTAAAACAC CCAGAGAAAC TCCCACTGGC TAACAAGGTG 60
GTGGCTTATT CACTTGCATT GGTTTTGCTC TTCTAGAAAC AGTAACCTGC CACCACCCTG 120
GTGTCTCTGG TGCCTTCTGC AAAGCACAGG TTTTATGGGC TGGGCCCAGC TCCCAGGGCA 180
CTGAGTATGG CCAGGCGGGT ACACCTGACT TGTACTGGGG TGACTGCAGG GTCTCTCAGA 240
CCTTAGCTCC TCCTCTGAAG AGCGGAAATG ACATGCAATT CTCTTGGGGT TGTAAAAATG 300
ACTAGATTAG ATGGTGCCAA ATCCCCAGTT CCTCCCCTAC TGCCATCAAG AGAGAGGAGA 360
GAGCAGAGAA TGCAAGGGAG TGCACAGACC TCACAGGTCA AGGGCTGCCT TGCTCACCTC 420
TGACATTAGC AGAGCTTGTT TCCTTACCTG TAAAACAAAG GTGGCGGGTT AGCTGTGAGG 480
TTTAAATGAC TTCCATGTAA AGAGTTAGAA GAGAGCCTGC AATGAGTGCT AAGCACATTC 540
ACCGTTTGTT TTCTCACGGG TTTTCTGTTA CACTCCTCCG AGTGCAGAGA GGCAGCTCCC 600
TTGTGAAGCT ATCCACACGG TCTTCCGCCT CTCGCTTGCC TGTCTCCTGT CTCTCCAGGG 660
AGGTGCTGGC TGCTGTTGGG CTGAGTCCTC TTGGAACTTC CTTGGGTTTC TTACACCAAC 720
ATTAAAGACT GAAGTAATCT CCCACCGCAG CCCCAGCCTC AAACTACTGC TCCTATTGTT 780
CCAGCCATCA TTTCTACACC CTGGGGTGGT TGTTCACATT CCTGGCTCAC TCATCTATCT 840
TCCTTCCTCC CCAAAGCTAT TCCCCTGACA TTCAGGCACA CTCCTTCCCC CTCATGCTTA 900
GATATGTGTC CCCAGTCCCT CTGGATATCC CTGCCAAATG TATCTTGCTA AACCCCCCTT 960
TTAAATTGGG ACACATCCCT CTAGTGGATA TCTGGATGCT GCCCTGTGTC TAGGGATCAA 1020
GCCCAACTCT TCCACTTGTG TAACTTATGG TGCTGCTTCC TGTGGTCATC TCAGTTCCCA 1080
CAGTTCCTAA CCCTTCTTCC CACTGCACAG 1110