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

TagContent
EnhancerAtlas ID
HS145-11782 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr19:41307630-41309280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs117391664chr1941309150hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr19:41308067-41308088GAAGCAGAAGGGGGAGGGTGG+6.18
ZNF263MA0528.1chr19:41308064-41308085GGAGAAGCAGAAGGGGGAGGG+6.81
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00640chr19:41303338-41314777Adipose_Nuclei
SE_01157chr19:41303447-41310550Adrenal_Gland
SE_03778chr19:41307637-41311042Brain_Angular_Gyrus
SE_04430chr19:41303263-41314995Brain_Anterior_Caudate
SE_05559chr19:41303199-41318218Brain_Cingulate_Gyrus
SE_06277chr19:41302932-41320507Brain_Hippocampus_Middle
SE_08430chr19:41305111-41319401Brain_Inferior_Temporal_Lobe
SE_09023chr19:41307770-41308261Brain_Mid_Frontal_Lobe
SE_09023chr19:41308269-41308495Brain_Mid_Frontal_Lobe
SE_09023chr19:41308607-41308894Brain_Mid_Frontal_Lobe
SE_09023chr19:41308965-41309492Brain_Mid_Frontal_Lobe
SE_11640chr19:41301961-41314911CD20
SE_12284chr19:41307705-41314600CD3
SE_14641chr19:41303241-41314926CD4_Memory_Primary_7pool
SE_17619chr19:41302314-41318336CD4p_CD25-_CD45RAp_Naive
SE_18094chr19:41302735-41315097CD4p_CD25-_CD45ROp_Memory
SE_20510chr19:41307642-41313854CD56
SE_21041chr19:41307063-41313770CD8_Memory_7pool
SE_22646chr19:41303127-41314598CD8_primiary
SE_24306chr19:41307704-41308374Colon_Crypt_2
SE_24306chr19:41308389-41311671Colon_Crypt_2
SE_27495chr19:41307644-41314787Esophagus
SE_28298chr19:41307702-41310593Fetal_Intestine
SE_29113chr19:41308025-41310759Fetal_Intestine_Large
SE_31926chr19:41307638-41314758Gastric
SE_40037chr19:41307668-41310220K562
SE_41247chr19:41303348-41314593Left_Ventricle
SE_42595chr19:41303119-41315055Lung
SE_46944chr19:41307760-41308416Ovary
SE_46944chr19:41308474-41310148Ovary
SE_50395chr19:41303125-41314958Sigmoid_Colon
SE_53239chr19:41307702-41314014Small_Intestine
SE_53554chr19:41303137-41314742Spleen
SE_65850chr19:41305247-41314690Pancreatic_islets
SE_69026chr19:41307690-41310641H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194130769241308431
Enhancer Sequence
GCAGGGTCAC AGGACAATAG TGGAGGGAAG GTCAGCAGAT AAACAAGTGA ACAGAGGTCT 60
CTGGTTTTCC TAGGCAGAGG ACCCTGCGGC CTTCTGCGTG TTTGTGTCCC TGGGTACTTG 120
AGATTAGGGA GTGGTGATGA CTCTTAACGA GCATGCTGCC TTCAAGCATC GCCACAGTGG 180
TTCTTGACTT TGCCAGGAAC CCTCTTAAAC TCATGAGAGC TGCTGACATT CACAGCGTGG 240
ACCTTGGTGG GGTTCATGGC CTCCTGGTGT CAGTCTGTGG CCCCAGACCA AGCACGGGGA 300
TGTAGATAGG CACACAGTTC ACCTGGCCGT TCTCTGTTGC TGTCTGTCCC TGTCCACATC 360
CTTCCCTGTG CTCCTGTCGT CCATCCCTGT TTGCTGGCCC ATGTTTCTAG TCCATCCATC 420
CTGTCTCCAA GGCAGGAGAA GCAGAAGGGG GAGGGTGGCT GTGATGAGTG AGCCCTGGGC 480
TGAGGGAAGG AAAGGGGTGC TGCCCGCTGG GCCGAGTGCT TGGCCCTGGA CTGCATTGTG 540
CCCTGGGTCC CCACTGTGGC ATCTGCATCG AGGACAGTCT CCTGGGGGTG GTACTGGGTG 600
GCTGCCTGTT GGCCCAGGTG GAGCTCATCC CCATGTCTCC CACCCTTCAC TGTCCCAGTC 660
CCTGCCCTCC ATTCCCCCTG TCCTGTGTGT CACTTCCTCC CTACCCATGT CTGTCTCTTC 720
CTCTGCCTTT ATGTGTTTGT TCTTAGTCCC TTTTTCTTTT TGCTTTAGAA CAATAGTTCT 780
TAATGGTATT TTGGAGCCTG GGTCTTTTTG AGAATCTGTC AGAGGCCACA GATCCTCTCT 840
TAAGACAAAT GCTCATTTGC TTGGAGTTTC CGGGCAGTTG TCAAGGCCTC ATGGCCTCCA 900
GCTGCCTGTT CAGGAACCTG GGGTCAGGAG CCCAGCACAG GACAGTGGTC CATAGGGCCT 960
TTCCGGGCTG CTGACAGGAT CATTGTCTTC ATGGGTGGTG TGGGGGCCTG GCCTTGAGTC 1020
CAAGGCTTGG TGTCCTTTGG ACAAGGCCCT GTGGGGAGTG CCCACTGCTC AACACAGTGA 1080
TGCCTGGCTG GCTGATGGCA CGGGCAGTGT TGTGCCCTGC AGGCGTGAGG CTGAGCTCCT 1140
GATGTCCTCT GCCTCCTCCT GCAGATCCCA TCTTGGGTTC TGCTTCTGTG TGGCTTTCCT 1200
CTCAGGCTGG AGCTGGCTCA GGGACCAGGG CTCCCCCGGG GCCAAGGCCT GTTTCCTCCC 1260
CACCCCAGCT GGAACTTGTT CTACTTCCCT CTCCCTCCCG TTACTTGATA GCTGAGCCAG 1320
AGCCGGCCCC TCCCTGGGCT TGGCTCCTGT GCGGGCGGGA TCAGTGGCCT CCCTGGCTCA 1380
GCATCTTCAC CCCAGGTTGG CTGTCGTCCT CGTCAGGGGG AGACCAGAAG GGCTGAGTGG 1440
CCCAGATGGG ACACTGCTCT GAGCCTCAAT TTGCTGATCC ACGGAATACG AAAACCAGGT 1500
TACATCCCCA GTGAGTCTGG CAGTTTGGGG AGGGGAGAGT AGGAGAAGAT CTCTTGTGTT 1560
TTGGTGCCTC TGGTGCCCAC TTTCTATGTG GTTGGGGACA GGGCCCCAGC GAGGATTGGG 1620
GAAGGGGCGT GTTTGGACTT TTTTAGCCCT 1650