EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS149-00537 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr17:48996170-48997700 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MafbMA0117.2chr17:48997580-48997592AGTCAGCAGTTT-6.22
RFX2MA0600.2chr17:48997194-48997210CATTGCCATGGAAACC+6.15
RFX2MA0600.2chr17:48997194-48997210CATTGCCATGGAAACC-6.18
RFX5MA0510.2chr17:48997194-48997210CATTGCCATGGAAACC-6.1
RFX5MA0510.2chr17:48997194-48997210CATTGCCATGGAAACC+6.24
RREB1MA0073.1chr17:48996249-48996269GGGGTGGGGTGGGGTGGGGG-6.74
RREB1MA0073.1chr17:48996248-48996268TGGGGTGGGGTGGGGTGGGG-7.67
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_02991chr17:48994624-48997228Bladder
SE_02991chr17:48997242-48997816Bladder
SE_03517chr17:48995128-48997800Brain_Angular_Gyrus
SE_04178chr17:48993971-48998112Brain_Anterior_Caudate
SE_05235chr17:48993417-48998834Brain_Cingulate_Gyrus
SE_06067chr17:48993102-48998709Brain_Hippocampus_Middle
SE_07466chr17:48993799-48998941Brain_Hippocampus_Middle_150
SE_08267chr17:48993505-48998192Brain_Inferior_Temporal_Lobe
SE_08899chr17:48996334-48997100Brain_Mid_Frontal_Lobe
SE_08899chr17:48997164-48997725Brain_Mid_Frontal_Lobe
SE_12167chr17:48995751-48997883CD3
SE_19619chr17:48992187-48997884CD4p_CD25-_Il17p_PMAstim_Th17
SE_23191chr17:48993461-48997830Colon_Crypt_1
SE_23784chr17:48993579-48997752Colon_Crypt_2
SE_24830chr17:48993475-48997727Colon_Crypt_3
SE_26011chr17:48995459-48999208Duodenum_Smooth_Muscle
SE_26691chr17:48991965-48997875Esophagus
SE_27621chr17:48994705-49002048Fetal_Intestine
SE_28540chr17:48994683-49002269Fetal_Intestine_Large
SE_29967chr17:48996231-48997810Fetal_Muscle
SE_31399chr17:48991729-48997856Gastric
SE_35088chr17:48996270-48997943HeLa
SE_37666chr17:48996166-48998175HSMMtube
SE_41117chr17:48994694-48997767Left_Ventricle
SE_42844chr17:48995090-48997815Lung
SE_47468chr17:48994886-48997790Pancreas
SE_49193chr17:48996258-48997806Right_Atrium
SE_49713chr17:48996488-48997655Right_Ventricle
SE_50311chr17:48993122-48997822Sigmoid_Colon
SE_52502chr17:48995428-48997845Small_Intestine
SE_54412chr17:48996674-48997693Spleen
SE_54634chr17:48995397-48999082Stomach_Smooth_Muscle
SE_57199chr17:48996702-48997718VACO_400
SE_59738chr17:48979175-49044314Ly4
SE_65373chr17:48993878-48999624Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr174899660048997689
chr174899694448997365
Number: 1             
IDChromosomeStartEnd
GH17I050914chr174899193349001980
Enhancer Sequence
AGCTCTGTGG ACACCTGAGG CCTCCTCCTG GAATTGCCCC AAGCCATGTG GCTAAGGCCT 60
AGGGAGACCC TCACCATGTG GGGTGGGGTG GGGTGGGGGC CCCTAGCCAA AGCTGGGAAA 120
AGGCAGAGCC TTCAGAGAGC CTCCTAGGGA CAGCAGCAGA GAGGAAGCCT TCGAGGCCTT 180
TCCAAGCTCC CCGCTGCCCG GCTCTCCTCC TGCCCAGCAC ACCGTGGGTG GACTCCAACC 240
TACAGCTTCA CTGATCTCAG AAGGTCCCAC CCTCTCCCGC CTTGTGCTTC TGACTGTTTA 300
TTTCCTGCAG AGGAGTCAGT GTTACTGCCA CTGAGAACAG AGATGGCTCC ACCCAGAGGG 360
CCCACCCTTG GGGCACAGGG GACCCTTGCC CATACCCCCT GCACCCTGGC TCCATCCTAA 420
TGCAGGGATA TGAGCTTGGG CCTGTGTCAC AGCTGCTTCC TGGGCCTCTG AATCCTCATC 480
CTTGAGCTGA GGGTGTGAGA CCGGAAAATC CAAGCCACCA TCCAGCCCCA ATGTCTCCCC 540
ATCCCATGAC TCTCTTCCCC AAATAACACA TCTCCCCAAA TACCTCTCCT CCTCCCCAGT 600
GAGAGGAGGC GCAGGGGAGG TTGTTGGATA ACTGTGCCTT CTCCTCCCCG AATCCCAGCC 660
TCTCCTTCTG GATCCCACAC CCAGGGGCCC AGCAGTCACG GGGCTCAGGG TGCTCCCCAG 720
CCTTTACAGT TTACCCATCC CTGCACAGTA GCCATGATTT CATTTCCTCC TCACTGCAAG 780
GTAAAGATCA TTAGTTCTCT TTTATAGGTG AAGAGACTTA GACTCAGACA GACCCTGTGT 840
CTTGCTCAAA GTCACCTGGC CAGTCAGGGG TAGGGCTGGG TTTCGAACCC AGGGGCAGGC 900
CCTCTCCGCC CCCCGGCATC GGTGCAGAGC CCTGGGTCGC CCTCCTCCAA GGTCGTTGTG 960
GTGTGAACAG CCAGGCGCCT TCATGCAGGG CCTGACTGCA GCCGCCAGAG CCTGGTGATG 1020
TCAGCATTGC CATGGAAACC CTTCCCCGGG CGTCGGGCAG GACCAGCCTC CCCAGCGCAG 1080
TTTCCCTTTG TGTGGACTTT GCAATGCGTT GCCAAGGCAG TGGGGCCTGC TGGGCGGGTT 1140
GGCATGGGGT GGGGAAGGCA GACAAAAACC CACACTGCAA CTGGCAGCTC ACAACAGGGC 1200
CCACGGTGCT TGTGGGAGGG AGGGGCTGCA GGCTGGTGGC CTAAGGCGTG AGAGTCGGTG 1260
GGCAGGGGGT TACCCACACA CCTGCTTAGG ACCCCCATCT GGCAACAGCC TTTTGGCGTC 1320
TTTGGTGCTA TTTTGGGGTC CTGCTGCCTA AGAATCACCT GGGCCTGGGT GTTGTGAAAA 1380
AGGCAGACCT GCTGGGCCGG GGTGGAGAGG AGTCAGCAGT TTAAACAAAC CCCCAAGGCA 1440
ATTCGCGTAT GCCACCAATT CCGAGGACAC CTTCAGGGAA GAATAACATT TATTGAGCAC 1500
CTAGCTATGC CAGGCAGGCC CTTCTGCCTA 1530