EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-46138 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr8:101474900-101475850 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs5893521chr8101475095hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MITFMA0620.2chr8:101475245-101475263GTAAGTCATGTGACCAGA+6.23
MITFMA0620.2chr8:101475245-101475263GTAAGTCATGTGACCAGA-6.23
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_18537chr8:101474767-101476978CD4p_CD25-_Il17-_PMAstim_Th
SE_19357chr8:101474800-101476994CD4p_CD25-_Il17p_PMAstim_Th17
SE_22743chr8:101474949-101476249CD8_primiary
SE_27991chr8:101475318-101476841Fetal_Intestine
SE_28830chr8:101475112-101476756Fetal_Intestine_Large
SE_32305chr8:101475087-101476367Gastric
SE_32533chr8:101474347-101477244GM12878
SE_34085chr8:101475071-101477112HCC1954
SE_47999chr8:101475715-101476254Pancreas
SE_62291chr8:101421434-101542088Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8101475207101475346
Number: 1             
IDChromosomeStartEnd
GH08I100462chr8101475138101477142
Enhancer Sequence
TAAATAAATA GTTGCATATG GAAAAGAAGT AGGAAACACC TTTCCAAAAC TAATAATATT 60
AACAAACTTC CAAGAGACAC ACAATCCATA ATTAGTGACT ATTTGGGGGG AAAAAAAGAC 120
ACAAACCTTG GAATTTGAAA TGTGATTCTG AGAACAGCCT GGTGTGTTTT TTCTTGCTCA 180
GAATCTGTCC ACCCTTTTTT TTTGGCCCCT TTCCCTTCTG ACAGCCACAT TAATTCAAAT 240
TCTTTCTCTA CATGTCTGTA GATTGCAAAT TTAGATACTG GGATTCAATA CTTCTTGCCT 300
GAACTCCCAG AGTCGCCAGT CGACAAAGGC TTATTAAAAA CCTCAGTAAG TCATGTGACC 360
AGACAGAACT GATTCTAGCT CAGCCCACAG GAAGGGTAGC CTTGCTCTCA GAAACCAAAT 420
CTCTGGCAAG GCTGCCTTTA GGGTCAGATT CAGTGACATT GGACTCCATG CTGGGGCAGA 480
CCCAATCGGT GTGCCTAGGC CAAGATTCAG CAGGCCACAG ATGCCTGGGG AATGAGCTTG 540
ACCTCCTGGA GTCACTCCTT AAGAGAAGCA CCCAGCCTAT ATCCCTGGGT TGTCCCACTT 600
CCAACACAGC CCATATAATG CTGAAATTCA TATGCCATTT ACTAACCTGT GCCAGATCAT 660
CATATCACCC TCCCCTCTTT CTCTCAAGTG TGGTAGAAAT GGCTAGTTGA CCCCTGAAAA 720
GTCATGATCT CCTTGACTCC TTGATCTGTA TAGTATGAAC TTGCTGTTGA GAAGCAGGTG 780
ACTAACCAGG GACTCCATTT CCCAGCCTCT CAACCCACCC CATGTCCTTC ACTCTGGCCA 840
GTGAAATAAG AGCCTGAGAG ATGTGTCACT TTCTGGCTGA GGTGGTTAAG TATCCAGTGT 900
GGCTTTCCTC ACTCTCTTCC CCAGCTTGTA TCACTAAAGG ACAGAGGCCT 950